Canonical Allele Identifier: PA204965
Gene: LMNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208980
ClinVar RCV Id: RCV000190899
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116126.3:p.His157Tyr
CA204964
NM_032737.4:c.469C>T