Canonical Allele Identifier: PA2826658926
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 502071
ClinVar RCV Id: RCV000592791 RCV001205747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg298Pro
CA342817795
NM_001282625.2:c.893G>C