Canonical Allele Identifier: PA2826659162
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48035
ClinVar RCV Id: RCV000057258 RCV000172002 RCV000157295 RCV000528639 RCV000769728 RCV000627127 RCV001172616 RCV002345327 RCV003996453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg401Cys
CA016870
NM_001282625.2:c.1201C>T