Allele Registry

Canonical Allele Identifier: PA217866

Gene: LMNA HGNC NCBI

ClinVar Allele:

77695

ClinVar RCV:

RCV000057261

RCV000694118

RCV000772169

RCV002281901

RCV002444514

RCV003996501

ClinVar Variation:

66798

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Leu421Pro	CA016923 NM_170708.4:c.1262T>C