Canonical Allele Identifier: PA2825515516
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 194094
ClinVar RCV Id: RCV000174376 RCV000724279 RCV001165659 RCV001165660
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Arg499Ser
CA239906
NM_001083885.3:c.1495C>A