Canonical Allele Identifier: PA2580107998
Gene: NAGLU HGNC NCBI

Linked Data

ClinVar Variation Id: 1951582
ClinVar RCV Id: RCV002686272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000254.2:p.Ser685Arg
CA399606013
NM_000263.4:c.2053A>C
CA399606022
NM_000263.4:c.2055T>A
CA399606024
NM_000263.4:c.2055T>G