Canonical Allele Identifier: PA2826563689
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024822
ClinVar RCV Id: RCV001325049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Asn129Asp
CA397836643
NM_001276698.3:c.385A>G