Canonical Allele Identifier: PA2830327898
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 3073956
ClinVar RCV Id: RCV004012498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ser463Pro
CA342822415
NM_170707.4:c.1387T>C