Allele Registry

Canonical Allele Identifier: PA2826658599

Gene: LMNA HGNC NCBI

ClinVar Allele:

77796

ClinVar RCV:

RCV000057404

RCV001258042

RCV001387327

RCV003996511

ClinVar Variation:

66899

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Ser143Pro	CA018081 NM_001282625.2:c.427T>C