Canonical Allele Identifier: PA2826658599
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ser143Pro
CA018081
NM_001282625.2:c.427T>C