Canonical Allele Identifier: PA2825515532
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 179975
ClinVar RCV Id: RCV000156778 RCV002492601 RCV003660765
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Leu524_Ter525insGlnArgProArgProGluGlyLeuProProLeuProSerProTrpSerGlnSerLeuSerThrValGlyPheIleLysLeuLeuAlaGlyLeuGlyLeuHisGlyGlnGlyGlyArgLysThrSerProLeuHisProSerProLeuAspGlnAsnTrpGluArgLysArgAlaGlyGlnGlyArgGlnLysValArgSerGlyThrGlyAlaValLeuGlyThrGln
CA185551
NM_001083885.3:c.1573T>C