Canonical Allele Identifier: PA2826659505
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66795
ClinVar RCV Id: RCV000057257 RCV000818990
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Pro4Arg
CA016863
NM_001282626.2:c.11C>G