Canonical Allele Identifier: PA095919
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 100707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Arg108His
CA235522
NM_000255.4:c.323G>A