Canonical Allele Identifier: PA915958620
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_000512.2:p.Cys551Tyr
CA234120
NM_000521.4:c.1652G>A