Canonical Allele Identifier: PA2829603587
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 242000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Asp364Asn
CA10581729
NM_005572.4:c.1090G>A