Allele Registry

Canonical Allele Identifier: PA103721

Gene: LMNA HGNC NCBI

ClinVar Allele:

77765

ClinVar RCV:

RCV000057365

RCV000503031

RCV001051802

ClinVar Variation:

66868

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg62Gly	CA017741 NM_170707.4:c.184C>G