Canonical Allele Identifier: PA658818617
Gene: LMNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542437
ClinVar RCV Id: RCV000652860 RCV000712223 RCV004025888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116126.3:p.Ala192Ser
CA9067840
NM_032737.4:c.574G>T