Canonical Allele Identifier: PA274873
Gene: TFAP2A HGNC NCBI

Linked Data

ClinVar Variation Id: 192350
ClinVar RCV Id: RCV000172980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035890.1:p.Arg213Ser
CA004715
NM_001042425.3:c.637C>A