Allele Registry

Canonical Allele Identifier: PA107783

Gene: NEU1 HGNC NCBI

ClinVar RCV:

RCV000002551

RCV003555898

ClinVar Variation:

2447

HGVS (amino-acid)	Matching Registered Transcripts
NP_000425.1:p.Leu363Pro	CA212559 NM_000434.4:c.1088T>C