Allele Registry

Canonical Allele Identifier: PA2826562508

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001984654

ClinVar Variation:

1434495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Gly120Val	CA397836868 NM_001276697.3:c.359G>T CA645588391 NM_001276697.3:c.359_360delinsTA