Canonical Allele Identifier: PA2825066551
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2124556
ClinVar RCV Id: RCV003057222 RCV003138455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Thr905Ser
CA401326972
NM_000152.5:c.2713A>T
CA401326976
NM_000152.5:c.2714C>G