Canonical Allele Identifier: PA2825963191
Gene: WDR81 HGNC NCBI

Linked Data

ClinVar Variation Id: 2606799
ClinVar RCV Id: RCV003354950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157281.1:p.Asp1185Glu
CA286873986
NM_001163809.2:c.3555C>G
CA397594709
NM_001163809.2:c.3555C>A