Allele Registry

Canonical Allele Identifier: PA123981

Gene: LMNB2 HGNC NCBI

ClinVar Allele:

29513

ClinVar RCV:

RCV000015561

RCV000057200

RCV000117496

RCV000551638

RCV000990135

RCV003224099

ClinVar Variation:

14474

HGVS (amino-acid)	Matching Registered Transcripts
NP_116126.3:p.Arg235Gln	CA123980 NM_032737.4:c.704G>A