Canonical Allele Identifier: PA2826659039
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2728396
ClinVar RCV Id: RCV003581262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Met352Thr
CA342820281
NM_001282625.2:c.1055T>C