Canonical Allele Identifier: PA136925
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45678
ClinVar RCV Id: RCV000038896 RCV002513513
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Ala207Ser
CA136924
NM_015404.4:c.619G>T