Allele Registry

Canonical Allele Identifier: PA2826443903

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000022641

RCV000057342

ClinVar Variation:

29775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg429Gly	CA017607 NM_001257374.3:c.1285C>G