Canonical Allele Identifier: PA2573266266
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1375663
ClinVar RCV Id: RCV001883407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Glu886Lys
CA198648756
NM_015404.4:c.2656G>A