Canonical Allele Identifier: PA2825207807
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_000512.2:p.Tyr266Asp
CA3305949
NM_000521.4:c.796T>G