Allele Registry

Canonical Allele Identifier: PA109569

Gene: TFAP2B HGNC NCBI

ClinVar RCV:

RCV000008510

ClinVar Variation:

8044

HGVS (amino-acid)	Matching Registered Transcripts
NP_003212.2:p.Pro73Arg	CA340721 NM_003221.4:c.218C>G