Canonical Allele Identifier: PA2826442900
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1705143
ClinVar RCV Id: RCV002281773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Met88Ile
CA342817007
NM_001257374.3:c.264G>A
CA342817008
NM_001257374.3:c.264G>C
CA342817009
NM_001257374.3:c.264G>T