Allele Registry

Canonical Allele Identifier: PA916003795

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000795724

RCV002487462

RCV003129840

ClinVar Variation:

331465

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258137.2:p.Arg5821His	CA1908205 NM_001271208.2:c.17462G>A