Canonical Allele Identifier: PA2826657817
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1422872
ClinVar RCV Id: RCV001926302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp289Asn
CA342820458
NM_001282624.2:c.865G>A