Canonical Allele Identifier: PA099548
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 3934
ClinVar RCV Id: RCV000004140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Gly454Ser
CA252932
NM_000520.6:c.1360G>A