Canonical Allele Identifier: PA2825360655
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 547801
ClinVar RCV Id: RCV000660304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027451.1:p.Arg248Gly
CA134048999
NM_001032280.3:c.742C>G