Allele Registry

Canonical Allele Identifier: PA2826659870

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001339043

ClinVar Variation:

1036090

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Ala147Ser	CA053444 NM_001282626.2:c.439G>T