Canonical Allele Identifier: PA915958566
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 372685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000512.2:p.Gly473Ser
CA3306126
NM_000521.4:c.1417G>A