Canonical Allele Identifier: PA2826659198
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 242002
ClinVar RCV Id: RCV000227837 RCV000597022 RCV001184022 RCV002479935 RCV003998891 RCV004020899
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg419Cys
CA049655
NM_001282625.2:c.1255C>T