Allele Registry

Canonical Allele Identifier: PA107879

Gene: NEU1 HGNC NCBI

ClinVar RCV:

RCV000002553

RCV000480504

RCV002281689

ClinVar Variation:

2449

HGVS (amino-acid)	Matching Registered Transcripts
NP_000425.1:p.Val217Met	CA115560 NM_000434.4:c.649G>A