Canonical Allele Identifier: PA2826659516
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1041658
ClinVar RCV Id: RCV001345496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg8Gly
CA342806015
NM_001282626.2:c.22C>G