Canonical Allele Identifier: PA915964942
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 665976
ClinVar RCV Id: RCV000824371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Arg891Leu
CA401326705
NM_001079804.3:c.2672G>T