Allele Registry

Canonical Allele Identifier: PA107722

Gene: NEU1 HGNC NCBI

ClinVar RCV:

RCV000002554

RCV000078816

ClinVar Variation:

2450

HGVS (amino-acid)	Matching Registered Transcripts
NP_000425.1:p.Gly243Arg	CA115561 NM_000434.4:c.727G>A CA363492139 NM_000434.4:c.727G>C