Canonical Allele Identifier: PA2826670406
Gene: TRMU HGNC NCBI

Linked Data

ClinVar Variation Id: 393172
ClinVar RCV Id: RCV000424646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269714.1:p.Phe82Leu
CA16608640
NM_001282785.2:c.246C>G
CA411940506
NM_001282785.2:c.244T>C
CA411940511
NM_001282785.2:c.246C>A