Canonical Allele Identifier: PA2825459607
Gene: GAA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.Pro39Thr
CA401360278
NM_001079803.3:c.115C>A