Canonical Allele Identifier: PA2826657866
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu306Pro
CA10584130
NM_001282624.2:c.917T>C