Canonical Allele Identifier: PA2830093631
Gene: CINP HGNC NCBI

Linked Data

ClinVar Variation Id: 402142
ClinVar RCV Id: RCV000454213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116019.1:p.Leu212_Ter213insGlyArgProGluThrAlaAlaAspThrGlySerPheHisValSerProGlyArgGlnSerAla
CA16609530
NM_032630.3:c.637T>G