Canonical Allele Identifier: PA2829823449
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 1026499
ClinVar RCV Id: RCV001326958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Val413Glu
CA374609091
NM_015404.4:c.1238T>A