Canonical Allele Identifier: PA2826659431
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1677884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Val538Ala
CA050838
NM_001282625.2:c.1613T>C