Allele Registry

Canonical Allele Identifier: PA220824

Gene: NEU1 HGNC NCBI

ClinVar RCV:

RCV000078815

ClinVar Variation:

93001

HGVS (amino-acid)	Matching Registered Transcripts
NP_000425.1:p.Ser182Arg	CA220823 NM_000434.4:c.544A>C CA363494027 NM_000434.4:c.546C>A CA363494038 NM_000434.4:c.546C>G