Canonical Allele Identifier: PA136901
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45664
ClinVar RCV Id: RCV000038882 RCV000291435 RCV000346369 RCV000477861 RCV000723700
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Ala64Asp
CA136900
NM_015404.4:c.191C>A