Canonical Allele Identifier: PA100378
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 1571
ClinVar RCV Id: RCV000001637 RCV001214384
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Arg482Trp
CA115054
NM_000263.4:c.1444C>T