Canonical Allele Identifier: PA149776
Gene: MVK HGNC NCBI

Linked Data

ClinVar Variation Id: 97564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000422.1:p.Thr356Met
CA149774
NM_000431.4:c.1067C>T