Canonical Allele Identifier: PA2829603701
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2773542
ClinVar RCV Id: RCV003532559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Thr394Ser
CA342820910
NM_005572.4:c.1180A>T
CA342820917
NM_005572.4:c.1181C>G