Canonical Allele Identifier: PA2826085456
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 937102
ClinVar RCV Id: RCV001206050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166896.1:p.Gly410Ser
CA5206007
NM_001173425.1:c.1228G>A