Canonical Allele Identifier: PA2826658028
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1475830
ClinVar RCV Id: RCV001976540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Met383Thr
CA342822432
NM_001282624.2:c.1148T>C