Canonical Allele Identifier: PA2580202938
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 2150882

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305754.1:p.Glu458Lys
CA7644713
NM_001318825.2:c.1372G>A