Canonical Allele Identifier: PA130495
Gene: MVK HGNC NCBI
ClinVar RCV:
RCV000032943
ClinVar Variation:
39728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.Leu41Pro
CA130493
NM_000431.4:c.122T>C