Canonical Allele Identifier: PA2827386875
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 194094
ClinVar RCV Id: RCV000174376 RCV000724279 RCV001165659 RCV001165660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333819.1:p.Arg531Ser
CA239906
NM_001346890.1:c.1591C>A