Canonical Allele Identifier: PA2826658334
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2098082
ClinVar RCV Id: RCV003019110
ClinVar Variation Id: 2431242
ClinVar RCV Id: RCV003140304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asn39Lys
CA342807688
NM_001282625.2:c.117T>A
CA342807691
NM_001282625.2:c.117T>G