Canonical Allele Identifier: PA210304
Gene: B9D1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217555
ClinVar RCV Id: RCV000201685 RCV000241546 RCV000778492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056496.1:p.Tyr32Cys
CA210301
NM_015681.6:c.95A>G