Canonical Allele Identifier: PA116621
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4035
ClinVar RCV Id: RCV000004250 RCV000664615 RCV002265547 RCV003329226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Ala237Val
CA116619
NM_001079803.3:c.710C>T