Canonical Allele Identifier: PA2826659309
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 3072513
ClinVar RCV Id: RCV004013535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Gly474Arg
CA342822565
NM_001282625.2:c.1420G>A
CA342822566
NM_001282625.2:c.1420G>C