Canonical Allele Identifier: PA2826443137
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Ala166Pro
CA342817513
NM_001257374.3:c.496G>C