Canonical Allele Identifier: PA658814550
Gene: WDR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 542762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079408.3:p.Cys1270Ser
CA95704883
NM_025132.4:c.3808T>A
CA356652320
NM_025132.4:c.3809G>C