Canonical Allele Identifier: PA2828467020
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068210
ClinVar RCV Id: RCV003991890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358995.1:p.Phe213Leu
CA362701560
NM_001372066.1:c.639C>G
CA362701561
NM_001372066.1:c.639C>A
CA362701570
NM_001372066.1:c.637T>C