Canonical Allele Identifier: PA2826660496
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_001269555.1:p.Arg439Cys
CA016991
NM_001282626.2:c.1315C>T