Allele Registry

Canonical Allele Identifier: PA2826443354

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003177761

ClinVar Variation:

2452987

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg239Ser	CA342820275 NM_001257374.3:c.717G>C CA342820276 NM_001257374.3:c.717G>T