Allele Registry

Canonical Allele Identifier: PA2826658061

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001238528

ClinVar Variation:

964333

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg401Gly	CA342822665 NM_001282624.2:c.1201C>G