Canonical Allele Identifier: PA2826658003
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg372Pro
CA017039
NM_001282624.2:c.1115G>C