Canonical Allele Identifier: PA2573062959
Gene: HEXB HGNC NCBI

Linked Data

ClinVar Variation Id: 1331374
ClinVar RCV Id: RCV001806718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000512.2:p.Arg100Gln
CA360062559
NM_000521.4:c.299G>A