Canonical Allele Identifier: PA2826659407
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66850
ClinVar RCV Id: RCV000057329 RCV000472329 RCV000499741 RCV001814041 RCV003483458
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Thr528Arg
CA017510
NM_001282625.2:c.1583C>G