Allele Registry

Canonical Allele Identifier: PA217706

Gene: LMNA HGNC NCBI

ClinVar Allele:

77662

ClinVar RCV:

RCV000057221

RCV000499410

RCV001231384

ClinVar Variation:

66765

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Leu35Pro	CA016503 NM_170707.4:c.104T>C