Canonical Allele Identifier: PA2826660001
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg216Cys
CA018379
NM_001282626.2:c.646C>T