Canonical Allele Identifier: PA103818
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 217451
ClinVar RCV Id: RCV000201431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Asp300Gly
CA10575804
NM_170707.4:c.899A>G