Canonical Allele Identifier: PA096278
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 1881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Gly717Val
CA249729
NM_000255.4:c.2150G>T