Canonical Allele Identifier: PA2826442960
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 264626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg108Cys
CA054046
NM_001257374.3:c.322C>T