Canonical Allele Identifier: PA1139725447
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 912452
ClinVar RCV Id: RCV001165661 RCV001165662 RCV001324966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Arg878Gln
CA5205565
NM_015404.4:c.2633G>A