Canonical Allele Identifier: PA2825064946
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2139403
ClinVar RCV Id: RCV003070816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser88Arg
CA401360559
NM_000152.5:c.262A>C
CA401360565
NM_000152.5:c.264C>A
CA401360566
NM_000152.5:c.264C>G