Canonical Allele Identifier: PA100469
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 1560
ClinVar RCV Id: RCV000001626 RCV000078455 RCV000817080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Arg674His
CA115042
NM_000263.4:c.2021G>A