Canonical Allele Identifier: PA2826659291
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 432879
ClinVar RCV Id: RCV000800973 RCV000725643 RCV000772026 RCV002395208 RCV002506209 RCV004003508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Met464Val
CA050209
NM_001282625.2:c.1390A>G