Allele Registry

Canonical Allele Identifier: PA218217

Gene: LMNA HGNC NCBI

ClinVar Allele:

77785

ClinVar RCV:

RCV000015599

RCV000057387

RCV000502816

RCV000622546

RCV000755005

ClinVar Variation:

66888

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Thr10Ile	CA017867 NM_170707.4:c.29C>T