Canonical Allele Identifier: PA104402
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66807
ClinVar RCV Id: RCV000057272 RCV000692072 RCV002468560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Tyr45Cys
CA017029
NM_170707.4:c.134A>G