Allele Registry

Canonical Allele Identifier: PA916022668

Gene: HEXA HGNC NCBI

ClinVar RCV:

RCV000806667

ClinVar Variation:

651332

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305754.1:p.Leu61Phe	CA393070269 NM_001318825.2:c.181C>T