Canonical Allele Identifier: PA2826659302
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14503
ClinVar RCV Id: RCV000015597 RCV000057293 RCV001246687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg471Cys
CA017213
NM_001282625.2:c.1411C>T