Canonical Allele Identifier: PA2826657732
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245682
ClinVar RCV Id: RCV000236116 RCV001176603 RCV001857795 RCV002379039 RCV003227732 RCV003998898
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg250Trp
CA10584124
NM_001282624.2:c.748C>T