Canonical Allele Identifier: PA915964568
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 371235
ClinVar RCV Id: RCV000410896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Met408Val
CA8815236
NM_001079804.3:c.1222A>G