Canonical Allele Identifier: PA2826658874
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ala278Pro
CA342817513
NM_001282625.2:c.832G>C