Canonical Allele Identifier: PA2825360586
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 192350
ClinVar RCV Id: RCV000172980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027451.1:p.Arg211Ser
CA004715
NM_001032280.3:c.631C>A