Canonical Allele Identifier: PA2826659091
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 408993
ClinVar RCV Id: RCV000458536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ile373Ser
CA16609888
NM_001282625.2:c.1118T>G