Canonical Allele Identifier: PA915964692
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 4032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Pro545Leu
CA116616
NM_001079804.3:c.1634C>T