Allele Registry

Canonical Allele Identifier: PA2826660296

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001302398

ClinVar Variation:

1005514

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg351Gly	CA342820271 NM_001282626.2:c.1051A>G