Canonical Allele Identifier: PA913198269
Gene: TRMU HGNC NCBI

Linked Data

ClinVar Variation Id: 597932
ClinVar RCV Id: RCV000734192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060476.2:p.Met219Val
CA10292154
NM_018006.5:c.655A>G