Canonical Allele Identifier: PA2826658221
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1058833
ClinVar RCV Id: RCV001368012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.His483Gln
CA342825856
NM_001282624.2:c.1449C>A
CA342825859
NM_001282624.2:c.1449C>G