Canonical Allele Identifier: PA116618
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4032
ClinVar RCV Id: RCV000004247 RCV001174962 RCV001785449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Pro545Leu
CA116616
NM_001079803.3:c.1634C>T