Canonical Allele Identifier: PA113628
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 403712
ClinVar RCV Id: RCV001782927 RCV000464818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro361Leu
CA8815163
NM_000152.5:c.1082C>T