Canonical Allele Identifier: PA136911
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45671
ClinVar RCV Id: RCV000038889 RCV000514950 RCV001167579 RCV001167578
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Thr77Ser
CA136910
NM_015404.4:c.229A>T
CA374613571
NM_015404.4:c.230C>G