Canonical Allele Identifier: PA2826816874
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_001278933.1:p.Gly324Arg
CA221070
NM_001292004.1:c.970G>A
CA360071975
NM_001292004.1:c.970G>C