Canonical Allele Identifier: PA2828245048
Gene: ZNF469 HGNC NCBI

Linked Data

ClinVar Variation Id: 3196007
ClinVar RCV Id: RCV004489816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354553.1:p.Leu3322Ile
CA397125319
NM_001367624.2:c.9964C>A