Canonical Allele Identifier: PA2825065835
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 2860705
ClinVar RCV Id: RCV003609078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Trp516Arg
CA401367152
NM_000152.5:c.1546T>A
CA401367153
NM_000152.5:c.1546T>C