Canonical Allele Identifier: PA104017
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Gly608Ser
CA015235
NM_170707.4:c.1822G>A