Allele Registry

Canonical Allele Identifier: PA2825206262

Gene: HEXA HGNC NCBI

ClinVar RCV:

RCV001913356

ClinVar Variation:

1402093

HGVS (amino-acid)	Matching Registered Transcripts
NP_000511.2:p.Ala20Val	CA7645121 NM_000520.6:c.59C>T