Allele Registry

Canonical Allele Identifier: PA2830396601

Gene: NIN HGNC NCBI

ClinVar RCV:

RCV000175357

RCV000989221

RCV002054066

ClinVar Variation:

194884

HGVS (amino-acid)	Matching Registered Transcripts
NP_891989.3:p.Gly1320Glu	CA201417 NM_182944.3:c.3959G>A