Canonical Allele Identifier: PA2825207310
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1037233
ClinVar RCV Id: RCV001340357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Arg424His
CA7644744
NM_000520.6:c.1271G>A