Canonical Allele Identifier: PA099472
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 3924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Asp258His
CA116509
NM_000520.6:c.772G>C