Canonical Allele Identifier: PA2829602724
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1014606
ClinVar RCV Id: RCV001313361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg11Leu
CA342806869
NM_005572.4:c.32G>T