Canonical Allele Identifier: PA2827037553
Gene: GLMN HGNC NCBI

Linked Data

ClinVar Variation Id: 298132
ClinVar RCV Id: RCV000349814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306612.1:p.Tyr353His
CA950390
NM_001319683.2:c.1057T>C