Canonical Allele Identifier: PA2826659502
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1058603
ClinVar RCV Id: RCV001367763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Pro4Ser
CA342805926
NM_001282626.2:c.10C>T