Canonical Allele Identifier: PA2826657869
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435771
ClinVar RCV Id: RCV000501231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg307Pro
CA342820778
NM_001282624.2:c.920G>C