Canonical Allele Identifier: PA2826085085
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 2405681
ClinVar RCV Id: RCV002789304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Tyr109Ser
CA374612863
NM_001173425.1:c.326A>C