Canonical Allele Identifier: PA1139670351
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 928929
ClinVar RCV Id: RCV001193578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Cys103Arg
CA401360685
NM_001079804.3:c.307T>C