Canonical Allele Identifier: PA2825460037
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 956244
ClinVar RCV Id: RCV001229014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Thr156Ser
CA401361558
NM_001079803.3:c.466A>T
CA401361565
NM_001079803.3:c.467C>G