Canonical Allele Identifier: PA2826660338
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1422872
ClinVar RCV Id: RCV001926302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp370Asn
CA342820458
NM_001282626.2:c.1108G>A