Canonical Allele Identifier: PA2826660147
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 285938
ClinVar RCV Id: RCV000390988 RCV000693559 RCV002250618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu284Pro
CA10605303
NM_001282626.2:c.851T>C