Canonical Allele Identifier: PA2825515422
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1929399
ClinVar RCV Id: RCV002642369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Gly374Arg
CA5205677
NM_001083885.3:c.1120G>A
CA374619940
NM_001083885.3:c.1120G>C