Allele Registry

Canonical Allele Identifier: PA210266

Gene: B9D1 HGNC NCBI

ClinVar Allele:

214356

ClinVar RCV:

RCV000201564

ClinVar Variation:

217554

HGVS (amino-acid)	Matching Registered Transcripts
NP_056496.1:p.Arg156Trp	CA210263 NM_015681.6:c.466C>T