Canonical Allele Identifier: PA2830054160
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484904
ClinVar RCV Id: RCV002008261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Met246Ile
CA2891692
NM_025132.4:c.738G>A
CA356634261
NM_025132.4:c.738G>T
CA356634262
NM_025132.4:c.738G>C