Allele Registry

Canonical Allele Identifier: PA103935

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015622

RCV000015623

RCV000057227

RCV000470514

RCV000502108

RCV001420791

ClinVar Variation:

14525

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Glu358Lys	CA016555 NM_170707.4:c.1072G>A