Canonical Allele Identifier: PA915958619
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 93200
ClinVar RCV Id: RCV000079062 RCV001854394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000512.2:p.Gly549Arg
CA221070
NM_000521.4:c.1645G>A
CA360071975
NM_000521.4:c.1645G>C