Canonical Allele Identifier: PA2826443771
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 497324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Gln381Pro
CA342822801
NM_001257374.3:c.1142A>C