Allele Registry

Canonical Allele Identifier: PA107816

Gene: NEU1 HGNC NCBI

ClinVar RCV:

RCV000002558

ClinVar Variation:

2454

HGVS (amino-acid)	Matching Registered Transcripts
NP_000425.1:p.Pro316Ser	CA115562 NM_000434.4:c.946C>T