Canonical Allele Identifier: PA149881
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 97612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.Thr237Ser
CA149879
NM_000431.4:c.709A>T
CA386649032
NM_000431.4:c.710C>G