Canonical Allele Identifier: PA2826660388
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu387Pro
CA10584130
NM_001282626.2:c.1160T>C