Canonical Allele Identifier: PA210342
Gene: B9D2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217556
ClinVar RCV Id: RCV000201776 RCV001844085 RCV002265681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085055.2:p.Gly155Ser
CA210341
NM_030578.4:c.463G>A