Canonical Allele Identifier: PA149785
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 97568
ClinVar RCV Id: RCV000083820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.Ser378Pro
CA149783
NM_000431.4:c.1132T>C