Canonical Allele Identifier: PA2825066208
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 656668
ClinVar RCV Id: RCV000813141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Ser686Lys
CA915952255
NM_000152.5:c.2057_2058delinsAA