Allele Registry

Canonical Allele Identifier: PA2826443909

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015603

RCV000057346

ClinVar Variation:

14509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Lys430Asn	CA017637 NM_001257374.3:c.1290G>C CA342825399 NM_001257374.3:c.1290G>T