Canonical Allele Identifier: PA2826658775
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66924
ClinVar RCV Id: RCV000057444 RCV001038356 RCV001535783
ClinVar Variation Id: 285122
ClinVar RCV Id: RCV000519005 RCV002521931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Gly232Arg
CA018465
NM_001282625.2:c.694G>C
CA10605004
NM_001282625.2:c.694G>A