Canonical Allele Identifier: PA645486908
Gene: MVD HGNC NCBI

Linked Data

ClinVar Variation Id: 253039
ClinVar RCV Id: RCV000239486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002452.1:p.Phe249Ser
CA8228757
NM_002461.3:c.746T>C