Canonical Allele Identifier: PA100446
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 1563
ClinVar RCV Id: RCV000001629 RCV001227283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Arg643His
CA250027
NM_000263.4:c.1928G>A