Allele Registry

Canonical Allele Identifier: PA204965

Gene: LMNB2 HGNC NCBI

ClinVar RCV:

RCV000190899

ClinVar Variation:

208980

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