Canonical Allele Identifier: PA2825065029
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 1999720
ClinVar RCV Id: RCV002819806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Tyr136Cys
CA401361124
NM_000152.5:c.407A>G