Canonical Allele Identifier: PA2826660002
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200964
ClinVar RCV Id: RCV000474813 RCV000778039 RCV001172621 RCV001775091 RCV002354479 RCV003996718 RCV000732408 RCV002478615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg216His
CA018387
NM_001282626.2:c.647G>A