Canonical Allele Identifier: PA2826443415
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48029
ClinVar RCV Id: RCV000041306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Met259_Ala263del
CA016606
NM_001257374.3:c.775_789del