Canonical Allele Identifier: PA100727
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 1570
ClinVar RCV Id: RCV000001636 RCV001851559 RCV003894784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Phe314Leu
CA115053
NM_000263.4:c.942C>G
CA290778701
NM_000263.4:c.940T>C
CA399600259
NM_000263.4:c.942C>A