Allele Registry

Canonical Allele Identifier: PA109511

Gene: TFAP2B HGNC NCBI

ClinVar RCV:

RCV000008505

ClinVar Variation:

8039

HGVS (amino-acid)	Matching Registered Transcripts
NP_003212.2:p.Ala275Asp	CA340716 NM_003221.4:c.824C>A