Canonical Allele Identifier: PA1139678671
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 914596
ClinVar RCV Id: RCV001168834 RCV001168835 RCV001236567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Gly6Glu
CA5206064
NM_001083885.3:c.17G>A