Canonical Allele Identifier: PA2826660621
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 242003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.His506Pro
CA10581731
NM_001282626.2:c.1517A>C