Canonical Allele Identifier: PA2826658454
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 543218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Tyr81His
CA342808404
NM_001282625.2:c.241T>C