Canonical Allele Identifier: PA175642
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 163051
ClinVar RCV Id: RCV000150392 RCV001037191 RCV001165948 RCV001165947 RCV001375239 RCV002483301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Thr383Asn
CA175641
NM_015404.4:c.1148C>A