Canonical Allele Identifier: PA915975968
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 97612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107657.1:p.Thr237Ser
CA149879
NM_001114185.3:c.709A>T
CA386649032
NM_001114185.3:c.710C>G