Canonical Allele Identifier: PA2826443701
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 3073956
ClinVar RCV Id: RCV004012498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Ser351Pro
CA342822415
NM_001257374.3:c.1051T>C