Canonical Allele Identifier: PA2826085190
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45678
ClinVar RCV Id: RCV000038896 RCV002513513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Ala207Ser
CA136924
NM_001173425.1:c.619G>T