Canonical Allele Identifier: PA658673552
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 446641
ClinVar RCV Id: RCV000516069 RCV001316218
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Gly495Arg
CA356631901
NM_025132.4:c.1483G>C