Canonical Allele Identifier: PA2825064822
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1433922
ClinVar RCV Id: RCV001984491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ala14Val
CA401360004
NM_000152.5:c.41C>T