Allele Registry

Canonical Allele Identifier: PA2826443352

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002295209

ClinVar Variation:

1722182

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ala238Val	CA342820270 NM_001257374.3:c.713C>T