Canonical Allele Identifier: PA2499281089
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 999430
ClinVar RCV Id: RCV001295427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Arg366Gly
CA374610306
NM_015404.4:c.1096C>G