Allele Registry

Canonical Allele Identifier: PA2826658692

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015572

RCV000057424

RCV000057425

RCV000211789

RCV000794743

ClinVar Variation:

14483

66913

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Asn195Lys	CA018269 NM_001282625.2:c.585C>A CA018275 NM_001282625.2:c.585C>G