Canonical Allele Identifier: PA2826660561
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66824
ClinVar RCV Id: RCV000057292 RCV002390204 RCV002514282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg471Gly
CA017206
NM_001282626.2:c.1411C>G