Allele Registry

Canonical Allele Identifier: PA2827086913

Gene: B9D1 HGNC NCBI

ClinVar RCV:

RCV000201685

RCV000241546

RCV000778492

ClinVar Variation:

217555

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308146.1:p.Tyr32Cys	CA210301 NM_001321217.2:c.95A>G