Allele Registry

Canonical Allele Identifier: PA306197

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000182360

RCV000208531

RCV000241819

RCV000528116

RCV000725540

RCV001778774

ClinVar Variation:

200938

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg216Cys	CA018379 NM_170707.4:c.646C>T