Canonical Allele Identifier: PA095939
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 218989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Arg369Cys
CA347895
NM_000255.4:c.1105C>T