Canonical Allele Identifier: PA145928
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 92692
ClinVar RCV Id: RCV000078456 RCV000604099 RCV000675734 RCV001516235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Arg737Ser
CA145927
NM_000263.4:c.2209C>A