Canonical Allele Identifier: PA174871
Gene: ZNF776 HGNC NCBI

Linked Data

ClinVar Variation Id: 161832
ClinVar RCV Id: RCV000149368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775903.3:p.Asn192His
CA174870
NM_173632.3:c.574A>C