Canonical Allele Identifier: PA2830329813
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 3072513
ClinVar RCV Id: RCV004013535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Gly474Arg
CA342822565
NM_170708.4:c.1420G>A
CA342822566
NM_170708.4:c.1420G>C