Canonical Allele Identifier: PA2830329132
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 937889
ClinVar RCV Id: RCV001207007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Asp164Tyr
CA342815632
NM_170708.4:c.490G>T