Canonical Allele Identifier: PA1139687805
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 838291
ClinVar RCV Id: RCV001039808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305754.1:p.Arg36Cys
CA393070537
NM_001318825.2:c.106C>T