Allele Registry

Canonical Allele Identifier: PA2826660298

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003177761

ClinVar Variation:

2452987

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg351Ser	CA342820275 NM_001282626.2:c.1053G>C CA342820276 NM_001282626.2:c.1053G>T