Canonical Allele Identifier: PA2826659288
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 3073956
ClinVar RCV Id: RCV004012498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ser463Pro
CA342822415
NM_001282625.2:c.1387T>C