Canonical Allele Identifier: PA113601
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 281052
ClinVar RCV Id: RCV000383868 RCV000723486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro285Ser
CA10603793
NM_000152.5:c.853C>T