ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952007
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.0498858495
Score
-0.4896068491
Score
0.9238110768
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000806895
RCV001019109
ClinVar Variation:
651517
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Asn310Asp
CA397836124
NM_000546.6:c.928A>G