Canonical Allele Identifier: PA145930
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 92693
ClinVar RCV Id: RCV000078457 RCV000588373 RCV000609064 RCV001523208 RCV001778706
ClinVar Variation Id: 971683
ClinVar RCV Id: RCV001247516
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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