Allele Registry

Canonical Allele Identifier: PA2826657860

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000248263

ClinVar Variation:

264271

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg305Thr	CA10587419 NM_001282624.2:c.914G>C