Canonical Allele Identifier: PA2826085204
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45681
ClinVar RCV Id: RCV000038899 RCV000279685 RCV000316099 RCV000839182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Arg223His
CA136928
NM_001173425.1:c.668G>A