Canonical Allele Identifier: PA2825066428
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1020834
ClinVar RCV Id: RCV001320484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Asn815Thr
CA401325230
NM_000152.5:c.2444A>C