Canonical Allele Identifier: PA2826657841
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14495
ClinVar RCV Id: RCV000503996 RCV000547164 RCV000681569 RCV000057235 RCV001089610 RCV002321484 RCV003319170
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg296His
CA016651
NM_001282624.2:c.887G>A