Canonical Allele Identifier: PA2826562862
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 135360
ClinVar RCV Id: RCV000122179 RCV000161039 RCV000991137 RCV000989697 RCV001356420 RCV001704037 RCV001798387 RCV003965030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ser207Ala
CA000036
NM_001276697.3:c.619T>G