Canonical Allele Identifier: PA2825601661
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024822
ClinVar RCV Id: RCV001325049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Asn288Asp
CA397836643
NM_001126112.3:c.862A>G