Canonical Allele Identifier: PA658679477
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 447702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg41Leu
CA342807753
NM_170708.4:c.122G>T