Canonical Allele Identifier: PA916019146
Gene: MVK HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288111.1:p.Leu41Pro
CA130493
NM_001301182.1:c.122T>C