Canonical Allele Identifier: PA2825515166
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1504000
ClinVar RCV Id: RCV002025864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Ser28Phe
CA374609125
NM_001083885.3:c.83C>T