Allele Registry

Canonical Allele Identifier: PA645396052

Gene: B9D2 HGNC NCBI

ClinVar RCV:

RCV000251213

RCV000616360

RCV000860230

RCV001668590

ClinVar Variation:

261881

HGVS (amino-acid)	Matching Registered Transcripts
NP_085055.2:p.Ile11Met	CA9460392 NM_030578.4:c.33A>G