Allele Registry

Canonical Allele Identifier: PA2826657774

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003177761

ClinVar Variation:

2452987

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg270Ser	CA342820275 NM_001282624.2:c.810G>C CA342820276 NM_001282624.2:c.810G>T