Canonical Allele Identifier: PA2825206884
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1921781
ClinVar RCV Id: RCV002613291

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.His262Arg
CA393063027
NM_000520.6:c.785A>G