Allele Registry

Canonical Allele Identifier: PA217889

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057265

RCV000148606

RCV000150953

RCV000653929

RCV001172619

RCV001524022

RCV002381364

ClinVar Variation:

66802

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Arg435Cys	CA014967 NM_170708.4:c.1303C>T