Allele Registry

Canonical Allele Identifier: PA2825206261

Gene: HEXA HGNC NCBI

ClinVar RCV:

RCV002715059

ClinVar Variation:

1954548

HGVS (amino-acid)	Matching Registered Transcripts
NP_000511.2:p.Ala20Gly	CA393070702 NM_000520.6:c.59C>G