Canonical Allele Identifier: PA2826657767
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 155896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Met267Ile
CA016471
NM_001282624.2:c.801G>T
CA342820261
NM_001282624.2:c.801G>A
CA342820262
NM_001282624.2:c.801G>C