Canonical Allele Identifier: PA1139678130
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 891628
ClinVar RCV Id: RCV001127040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Gly119Arg
CA399596259
NM_000263.4:c.355G>A
CA399596261
NM_000263.4:c.355G>C