Canonical Allele Identifier: PA915958587
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 435415
ClinVar RCV Id: RCV000502357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000512.2:p.Arg533Cys
CA3306210
NM_000521.4:c.1597C>T