Allele Registry

Canonical Allele Identifier: PA217802

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057244

ClinVar Variation:

66783

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg386Met	CA016743 NM_170707.4:c.1157G>T