Canonical Allele Identifier: PA658827385
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 554870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Arg393Gln
CA7644763
NM_000520.6:c.1178G>A