Canonical Allele Identifier: PA891857302
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 576229
ClinVar RCV Id: RCV000698675 RCV001183323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.His163Gln
CA342815625
NM_170708.4:c.489T>A
CA342815627
NM_170708.4:c.489T>G