Canonical Allele Identifier: PA2826669755
Gene: TRMU HGNC NCBI

Linked Data

ClinVar Variation Id: 1193998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269711.1:p.Gly111Arg
CA411946152
NM_001282782.2:c.331G>A
CA411946153
NM_001282782.2:c.331G>C