Canonical Allele Identifier: PA136882
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 45654
ClinVar RCV Id: RCV000038872 RCV000888343 RCV001165874 RCV001165873
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056219.3:p.Pro485Leu
CA136881
NM_015404.4:c.1454C>T