Canonical Allele Identifier: PA2825066062
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2441621
ClinVar RCV Id: RCV003144096 RCV003237380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Trp621Arg
CA401369674
NM_000152.5:c.1861T>A
CA401369676
NM_000152.5:c.1861T>C