Canonical Allele Identifier: PA2826658170
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1677884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Val457Ala
CA050838
NM_001282624.2:c.1370T>C