Canonical Allele Identifier: PA2826658202
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2773549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp472His
CA342825579
NM_001282624.2:c.1414G>C