Canonical Allele Identifier: PA136927
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45680
ClinVar RCV Id: RCV000038898 RCV000961958 RCV001166012 RCV001166013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Arg223Cys
CA136926
NM_015404.4:c.667C>T