Allele Registry

Canonical Allele Identifier: PA2826443473

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057244

ClinVar Variation:

66783

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg274Met	CA016743 NM_001257374.3:c.821G>T