Canonical Allele Identifier: PA915959261
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 547801
ClinVar RCV Id: RCV000660304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035890.1:p.Arg250Gly
CA134048999
NM_001042425.3:c.748C>G