Canonical Allele Identifier: PA2826659162
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg401Cys
CA016870
NM_001282625.2:c.1201C>T