Canonical Allele Identifier: PA2826443705
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 432879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Met352Val
CA050209
NM_001257374.3:c.1054A>G