Allele Registry

Canonical Allele Identifier: PA2826443353

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057220

RCV003581571

ClinVar Variation:

66764

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ala238Pro	CA016496 NM_001257374.3:c.712G>C