Canonical Allele Identifier: PA149932
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 97638
ClinVar RCV Id: RCV000083891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.Thr322Ser
CA149930
NM_000431.4:c.965C>G
CA386650709
NM_000431.4:c.964A>T