Canonical Allele Identifier: PA306198
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200938
ClinVar RCV Id: RCV000182360 RCV000241819 RCV000208531 RCV000528116 RCV001778774 RCV000725540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg216Cys
CA018379
NM_170708.4:c.646C>T