Canonical Allele Identifier: PA915964136
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 594278
ClinVar RCV Id: RCV000729535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Pro39Leu
CA401360282
NM_001079804.3:c.116C>T