Canonical Allele Identifier: PA2826659953
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14483
ClinVar Variation Id: 66913
ClinVar RCV Id: RCV000057424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asn195Lys
CA018269
NM_001282626.2:c.585C>A
CA018275
NM_001282626.2:c.585C>G