Canonical Allele Identifier: PA2826444020
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 162411
ClinVar RCV Id: RCV000192014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Cys479Ser
CA347053
NM_001257374.3:c.1435T>A
CA342826702
NM_001257374.3:c.1436G>C