Allele Registry

Canonical Allele Identifier: PA217887

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057265

RCV000148606

RCV000150953

RCV000653929

RCV001172619

RCV001524022

RCV002381364

ClinVar Variation:

66802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg323Cys	CA014967 NM_001257374.3:c.967C>T