Canonical Allele Identifier: PA198785
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 188479
ClinVar RCV Id: RCV001042621 RCV002408727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Val357Phe
CA198782
NM_001079803.3:c.1069G>T