Canonical Allele Identifier: PA916048829
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 807514
ClinVar RCV Id: RCV000995666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358995.1:p.Leu251Pro
CA362701169
NM_001372066.1:c.752T>C