Allele Registry

Canonical Allele Identifier: PA148261

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000081143

RCV000361795

RCV000589805

RCV001542875

ClinVar Variation:

95137

HGVS (amino-acid)	Matching Registered Transcripts
NP_004534.2:p.Lys2613Asn	CA148258 NM_004543.4:c.7839G>C CA348781478 NM_004543.4:c.7839G>T