Allele Registry

Canonical Allele Identifier: PA2826999735

Gene: HEXA HGNC NCBI

ClinVar RCV:

RCV004404363

ClinVar Variation:

3105522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305754.1:p.Asp62Tyr	CA393070258 NM_001318825.2:c.184G>T