Canonical Allele Identifier: PA096299
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 167312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Gly94Arg
CA234291
NM_000255.4:c.280G>A
CA364405089
NM_000255.4:c.280G>C