Allele Registry

Canonical Allele Identifier: PA107848

Gene: NEU1 HGNC NCBI

ClinVar RCV:

RCV000492831

RCV000781657

ClinVar Variation:

430337

HGVS (amino-acid)	Matching Registered Transcripts
NP_000425.1:p.Ser182Gly	CA3725021 NM_000434.4:c.544A>G