Canonical Allele Identifier: PA149788
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 97569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.His380Arg
CA149786
NM_000431.4:c.1139A>G