Canonical Allele Identifier: PA279488
Gene: B9D2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217558
ClinVar RCV Id: RCV000201694 RCV001844086 RCV002265683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_085055.2:p.Pro74Ser
CA279487
NM_030578.4:c.220C>T