Canonical Allele Identifier: PA916022744
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 554870
ClinVar RCV Id: RCV000670578 RCV001002010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305754.1:p.Arg404Gln
CA7644763
NM_001318825.2:c.1211G>A