Allele Registry

Canonical Allele Identifier: PA2826442754

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001339043

ClinVar Variation:

1036090

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ala35Ser	CA053444 NM_001257374.3:c.103G>T