Canonical Allele Identifier: PA2828245022
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232888
ClinVar RCV Id: RCV004523520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Gly3284Trp
CA397124897
NM_001367624.2:c.9850G>T