Canonical Allele Identifier: PA2826085464
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1026499
ClinVar RCV Id: RCV001326958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Val413Glu
CA374609091
NM_001173425.1:c.1238T>A