Allele Registry

Canonical Allele Identifier: PA2826443297

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001775173

ClinVar Variation:

1077066

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg219Leu	CA342820152 NM_001257374.3:c.656G>T