Canonical Allele Identifier: PA2826443060
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66931
ClinVar RCV Id: RCV000057453 RCV000201012 RCV000501991 RCV000496185 RCV000548477 RCV000662104 RCV001814042 RCV003230389 RCV004018991
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg137Gln
CA018567
NM_001257374.3:c.410G>A