Canonical Allele Identifier: PA2826669987
Gene: TRMU HGNC NCBI

Linked Data

ClinVar Variation Id: 1193998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269712.1:p.Gly85Arg
CA411946152
NM_001282783.2:c.253G>A
CA411946153
NM_001282783.2:c.253G>C