Allele Registry

Canonical Allele Identifier: PA2826443475

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000248263

ClinVar Variation:

264271

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg274Thr	CA10587419 NM_001257374.3:c.821G>C