Canonical Allele Identifier: PA891857376
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 580670
ClinVar RCV Id: RCV000704281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Ile373Met
CA342820516
NM_170708.4:c.1119C>G