Canonical Allele Identifier: PA217962
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Ile46Val
CA017105
NM_170708.4:c.136A>G