Canonical Allele Identifier: PA915976050
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 11929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107657.1:p.Val377Ile
CA121776
NM_001114185.3:c.1129G>A