Canonical Allele Identifier: PA2826442738
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Ser31Pro
CA018081
NM_001257374.3:c.91T>C