Canonical Allele Identifier: PA916018436
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 381669
ClinVar RCV Id: RCV000427051 RCV000669074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278933.1:p.Tyr41Asp
CA3305949
NM_001292004.1:c.121T>G