Canonical Allele Identifier: PA658818620
Gene: LMNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542428
ClinVar RCV Id: RCV000652851 RCV001532366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116126.3:p.Arg234Trp
CA9067792
NM_032737.4:c.700C>T