Canonical Allele Identifier: PA2826659818
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2587216
ClinVar RCV Id: RCV003360741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Lys123Asn
CA342815028
NM_001282626.2:c.369G>T
CA342815032
NM_001282626.2:c.369G>C