Allele Registry

Canonical Allele Identifier: PA2826659120

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000248263

ClinVar Variation:

264271

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Arg386Thr	CA10587419 NM_001282625.2:c.1157G>C