Allele Registry

Canonical Allele Identifier: PA217395

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057045

RCV000790249

RCV001176130

RCV001854169

RCV002504958

RCV003996491

ClinVar Variation:

66611

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Arg571Cys	CA017701 NM_005572.4:c.1711C>T