Canonical Allele Identifier: PA218441
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14524
ClinVar Variation Id: 543181
ClinVar RCV Id: RCV000653857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg249Trp
CA018559
NM_170708.4:c.745C>T
CA658795529
NM_170708.4:c.744_745delinsTT