Canonical Allele Identifier: PA2826816877
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 167176
ClinVar RCV Id: RCV000153360 RCV000674784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278933.1:p.Cys326Tyr
CA234120
NM_001292004.1:c.977G>A