Canonical Allele Identifier: PA2826085122
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 179995
ClinVar RCV Id: RCV000156798 RCV000936540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Glu137Gln
CA185597
NM_001173425.1:c.409G>C