Canonical Allele Identifier: PA2825616077
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024822
ClinVar RCV Id: RCV001325049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Asn156Asp
CA397836643
NM_001126117.1:c.466A>G