Canonical Allele Identifier: PA100890
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 371634
ClinVar RCV Id: RCV000409594 RCV000626636 RCV000705481 RCV002275001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Tyr140Cys
CA8576764
NM_000263.4:c.419A>G