Canonical Allele Identifier: PA2826660750
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1329343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ser571Asn
CA342826307
NM_001282626.2:c.1712G>A