Canonical Allele Identifier: PA645457772
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 242000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Asp364Asn
CA10581729
NM_170708.4:c.1090G>A