Allele Registry

Canonical Allele Identifier: PA2826657861

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057244

ClinVar Variation:

66783

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg305Met	CA016743 NM_001282624.2:c.914G>T