Canonical Allele Identifier: PA217939
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Asn456Asp
CA017074
NM_005572.4:c.1366A>G