Canonical Allele Identifier: PA2826658407
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66868
ClinVar RCV Id: RCV000057365 RCV000503031 RCV001051802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg62Gly
CA017741
NM_001282625.2:c.184C>G