Canonical Allele Identifier: PA2825207317
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1468401
ClinVar RCV Id: RCV001968964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Ser426Phe
CA393060645
NM_000520.6:c.1277C>T