Canonical Allele Identifier: PA915959257
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 547799
ClinVar RCV Id: RCV000660302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035890.1:p.Leu234Pro
CA362701241
NM_001042425.3:c.701T>C