Canonical Allele Identifier: PA2826660056
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 634638
ClinVar RCV Id: RCV000785172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp243Tyr
CA342817279
NM_001282626.2:c.727G>T