Allele Registry

Canonical Allele Identifier: PA2826657776

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001302398

ClinVar Variation:

1005514

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg270Gly	CA342820271 NM_001282624.2:c.808A>G