Canonical Allele Identifier: PA2827386542
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1489867
ClinVar RCV Id: RCV001983472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Ala107Thr
CA5205981
NM_001346890.1:c.319G>A