Canonical Allele Identifier: PA113636
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 456370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Pro397Leu
CA8815197
NM_000152.5:c.1190C>T