Canonical Allele Identifier: PA2830325902
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 655012
ClinVar RCV Id: RCV000811094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg48Leu
CA342807945
NM_170707.4:c.143G>T