Canonical Allele Identifier: PA1139729438
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 937102
ClinVar RCV Id: RCV001206050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Gly59Ser
CA5206007
NM_001346890.1:c.175G>A