Canonical Allele Identifier: PA2826659197
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 476822
ClinVar RCV Id: RCV000549013 RCV001172620 RCV002420529 RCV002483493 RCV003999467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg419His
CA049674
NM_001282625.2:c.1256G>A