Canonical Allele Identifier: PA2826443652
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Asp334Val
CA017008
NM_001257374.3:c.1001A>T