Canonical Allele Identifier: PA099354
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 3925
ClinVar RCV Id: RCV000004131 RCV002345229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Arg170Trp
CA252927
NM_000520.6:c.508C>T