Canonical Allele Identifier: PA121786
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 11933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.Pro165Leu
CA121784
NM_000431.4:c.494C>T