Allele Registry

Canonical Allele Identifier: PA916004158

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000292919

RCV000535305

RCV002502095

RCV002518819

ClinVar Variation:

281478

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258137.2:p.Ala6885Val	CA1907204 NM_001271208.2:c.20654C>T