ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952019
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.5929365516
Score
0.6657643967
Score
-0.615041611
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001995379
ClinVar Variation:
1471105
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Pro309Leu
CA397836130
NM_000546.6:c.926C>T