Canonical Allele Identifier: PA658818629
Gene: LMNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542438
ClinVar RCV Id: RCV000652861 RCV004025889
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116126.3:p.Arg438Trp
CA9067535
NM_032737.4:c.1312C>T