Canonical Allele Identifier: PA915958522
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 397589
ClinVar RCV Id: RCV000449491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000512.2:p.Arg100Pro
CA16609444
NM_000521.4:c.299G>C