Canonical Allele Identifier: PA645376303
Gene: B9D1 HGNC NCBI

Linked Data

ClinVar Variation Id: 386519
ClinVar RCV Id: RCV000427074
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056496.1:p.Gly165Cys
CA16608390
NM_015681.6:c.493G>T