Canonical Allele Identifier: PA2826660749
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 854390
ClinVar RCV Id: RCV001059431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ser568Cys
CA342826240
NM_001282626.2:c.1703C>G