Canonical Allele Identifier: PA645481608
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 255365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Val220Leu
CA8814955
NM_000152.5:c.658G>T
CA401362471
NM_000152.5:c.658G>C