Canonical Allele Identifier: PA915959250
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 445515
ClinVar RCV Id: RCV000514793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035890.1:p.Val176Met
CA362701957
NM_001042425.3:c.526G>A