Canonical Allele Identifier: PA217894
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66804
ClinVar RCV Id: RCV000057267 RCV001225469 RCV001182564 RCV002381365 RCV003996503 RCV003326119 RCV004537256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg439Cys
CA016991
NM_170708.4:c.1315C>T