ClinGen Allele Registry
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Canonical Allele Identifier:
PA107344
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.9305344123
Score
-1.2014883956
Score
1.066360923
Score
0.265312565
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000214341
RCV000223396
RCV000418173
RCV000418768
RCV000418817
RCV000423333
RCV000423542
RCV000424469
RCV000429546
RCV000429913
RCV000433605
RCV000434638
RCV000435180
RCV000435365
RCV000439338
RCV000440133
RCV000441217
RCV000477355
RCV000785308
RCV001255635
ClinVar Variation:
233951
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val173Met
CA10577579
NM_000546.6:c.517G>A