Canonical Allele Identifier: PA2826657419
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66906
ClinVar RCV Id: RCV000057417 RCV000148603 RCV000794744 RCV001177403 RCV001775077 RCV002345365 RCV002477186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg108Trp
CA014940
NM_001282624.2:c.322C>T