Canonical Allele Identifier: PA2825206425
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1896094
ClinVar RCV Id: RCV002569634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Val60Ala
CA393070273
NM_000520.6:c.179T>C