Allele Registry

Canonical Allele Identifier: PA2826660001

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000182360

RCV000208531

RCV000241819

RCV000528116

RCV000725540

RCV001778774

ClinVar Variation:

200938

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg216Cys	CA018379 NM_001282626.2:c.646C>T