Allele Registry

Canonical Allele Identifier: PA2826535488

Gene: NEB HGNC NCBI

ClinVar RCV:

RCV000641337

RCV001662690

RCV002507092

ClinVar Variation:

533993

HGVS (amino-acid)	Matching Registered Transcripts
NP_001258137.2:p.Arg2437Trp	CA1909881 NM_001271208.2:c.7309C>T