Canonical Allele Identifier: PA2826563692
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172923
ClinVar RCV Id: RCV001527090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Leu130Pro
CA397836609
NM_001276698.3:c.389T>C