Canonical Allele Identifier: PA170086
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 143187
ClinVar RCV Id: RCV000132721 RCV001378699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Trp649Leu
CA170085
NM_000263.4:c.1946G>T