Canonical Allele Identifier: PA145930
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 92693
ClinVar Variation Id: 971683
ClinVar RCV Id: RCV001247516

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Arg737Gly
CA145929
NM_000263.4:c.2209C>G
CA1139665544
NM_000263.4:c.2208_2209delinsTG