Allele Registry

Canonical Allele Identifier: PA103392

Gene: LMNA HGNC NCBI

ClinVar Allele:

77825

ClinVar RCV:

RCV000057449

RCV001048135

RCV002381367

ClinVar Variation:

66928

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg25Gly	CA018531 NM_170707.4:c.73C>G