Canonical Allele Identifier: PA2499249973
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1026499
ClinVar RCV Id: RCV001326958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Val62Glu
CA374609091
NM_001346890.1:c.185T>A