Canonical Allele Identifier: PA136915
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45673
ClinVar RCV Id: RCV000038891 RCV001169716 RCV001204993 RCV001169715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Thr785Ile
CA136914
NM_015404.4:c.2354C>T