Canonical Allele Identifier: PA2825369730
Gene: GLUL HGNC NCBI

Linked Data

ClinVar Variation Id: 376910
ClinVar RCV Id: RCV000422703 RCV004022263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028228.1:p.Gly172Ala
CA16603208
NM_001033056.4:c.515G>C