Canonical Allele Identifier: PA1139670562
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 840069
ClinVar RCV Id: RCV001041971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Asn177Thr
CA294887368
NM_001079804.3:c.530A>C