Canonical Allele Identifier: PA2825206490
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 2118752
ClinVar RCV Id: RCV003030636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000511.2:p.Ser77Ala
CA393070088
NM_000520.6:c.229T>G