Canonical Allele Identifier: PA116768
Gene: GBA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005741.1:p.Asn409Ser
CA116767
NM_001005741.2:c.1226A>G