Canonical Allele Identifier: PA248170
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 199137
ClinVar RCV Id: RCV000218629 RCV000724324 RCV003947539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Val735Ile
CA248169
NM_015404.4:c.2203G>A