Canonical Allele Identifier: PA2829823443
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 937102
ClinVar RCV Id: RCV001206050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Gly410Ser
CA5206007
NM_015404.4:c.1228G>A