Allele Registry

Canonical Allele Identifier: PA2829603613

Gene: LMNA HGNC NCBI

ClinVar Allele:

490402

ClinVar RCV:

RCV000592581

RCV000696116

ClinVar Variation:

498978

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Glu372Lys	CA342820494 NM_005572.4:c.1114G>A