Canonical Allele Identifier: PA915958575
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 3879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000512.2:p.Arg505Gln
CA116487
NM_000521.4:c.1514G>A