Canonical Allele Identifier: PA2825079625
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 3178085
ClinVar RCV Id: RCV004472474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Glu415Val
CA364398807
NM_000255.4:c.1244A>T