Canonical Allele Identifier: PA2826659490
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200928
ClinVar RCV Id: RCV000182349 RCV000664076 RCV000778037 RCV001701632 RCV004020193 RCV000852591 RCV001852310 RCV002464010
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg571His
CA017707
NM_001282625.2:c.1712G>A