Canonical Allele Identifier: PA915964815
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 656668
ClinVar RCV Id: RCV000813141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Ser686Lys
CA915952255
NM_001079804.3:c.2057_2058delinsAA