Canonical Allele Identifier: PA2826659488
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 449051
ClinVar RCV Id: RCV000519351 RCV001524187 RCV004527626 RCV003581682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Val567Leu
CA342825921
NM_001282625.2:c.1699G>C
CA342825922
NM_001282625.2:c.1699G>T