Canonical Allele Identifier: PA2826670039
Gene: TRMU HGNC NCBI

Linked Data

ClinVar Variation Id: 441106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269712.1:p.Arg154Trp
CA10292309
NM_001282783.2:c.460C>T