Allele Registry

Canonical Allele Identifier: PA272897

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000148599

RCV000182377

RCV000245708

RCV000725647

RCV000769735

RCV001079490

RCV001330501

ClinVar Variation:

161291

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg644His	CA014889 NM_170707.4:c.1931G>A