Allele Registry

Canonical Allele Identifier: PA916004691

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000081132

RCV000398581

RCV000587497

RCV000693166

RCV001542973

RCV002499240

ClinVar Variation:

95126

571908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258137.2:p.Ile8437Val	CA148226 NM_001271208.2:c.25309A>G CA891842684 NM_001271208.2:c.25308_25309delinsTG