Canonical Allele Identifier: PA184258
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 179353
ClinVar RCV Id: RCV000156142 RCV001168958 RCV001422011 RCV001168959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Gly7Arg
CA184257
NM_015404.4:c.19G>C