Canonical Allele Identifier: PA2826660297
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2773540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg351Lys
CA048892
NM_001282626.2:c.1052G>A