Canonical Allele Identifier: PA2830326406
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 926737
ClinVar RCV Id: RCV001189543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Ile128Thr
CA053305
NM_170707.4:c.383T>C