Canonical Allele Identifier: PA2827087124
Gene: B9D1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308147.1:p.Tyr32Cys
CA210301
NM_001321218.2:c.95A>G