Canonical Allele Identifier: PA1139670535
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 956244
ClinVar RCV Id: RCV001229014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Thr156Ser
CA401361558
NM_001079804.3:c.466A>T
CA401361565
NM_001079804.3:c.467C>G