Canonical Allele Identifier: PA2826659132
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 408997
ClinVar RCV Id: RCV000476791 RCV001753890
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg388_Pro393dup
CA16609880
NM_001282625.2:c.1161_1178dup