Allele Registry

Canonical Allele Identifier: PA109523

Gene: TFAP2B HGNC NCBI

ClinVar RCV:

RCV000008507

ClinVar Variation:

8041

HGVS (amino-acid)	Matching Registered Transcripts
NP_003212.2:p.Arg236Cys	CA340718 NM_003221.4:c.706C>T