Canonical Allele Identifier: PA2826085393
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 288922
ClinVar RCV Id: RCV000271876 RCV000330120 RCV000366983 RCV000880644 RCV003940063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Val359Ile
CA5206087
NM_001173425.1:c.1075G>A