Canonical Allele Identifier: PA210286
Gene: B9D2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217557
ClinVar RCV Id: RCV000201607 RCV002265682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085055.2:p.Leu36Pro
CA210285
NM_030578.4:c.107T>C