Canonical Allele Identifier: PA2829603925
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 432879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Met464Val
CA050209
NM_005572.4:c.1390A>G