Canonical Allele Identifier: PA2827037532
Gene: GLMN HGNC NCBI

Linked Data

ClinVar Variation Id: 298145
ClinVar RCV Id: RCV000269071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001306612.1:p.Ala146Val
CA950588
NM_001319683.2:c.437C>T