Canonical Allele Identifier: PA2825460659
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 281052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Pro285Ser
CA10603793
NM_001079803.3:c.853C>T