Canonical Allele Identifier: PA095950
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 203846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Arg369His
CA312764
NM_000255.4:c.1106G>A