Canonical Allele Identifier: PA100937
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 92691
ClinVar RCV Id: RCV000078454 RCV001854380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Tyr455Cys
CA220552
NM_000263.4:c.1364A>G