Canonical Allele Identifier: PA2826657771
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66762
ClinVar RCV Id: RCV000057218 RCV000500548 RCV000653911 RCV000845011 RCV000754811 RCV002504959 RCV003996495
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg268Trp
CA016479
NM_001282624.2:c.802C>T