Canonical Allele Identifier: PA185598
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 179995
ClinVar RCV Id: RCV000156798 RCV000936540
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Glu137Gln
CA185597
NM_015404.4:c.409G>C