Allele Registry

Canonical Allele Identifier: PA2826658995

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001775173

ClinVar Variation:

1077066

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Arg331Leu	CA342820152 NM_001282625.2:c.992G>T