Canonical Allele Identifier: PA2826443738
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1522462
ClinVar RCV Id: RCV002034441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Asp363Gly
CA342822584
NM_001257374.3:c.1088A>G