Canonical Allele Identifier: PA174142
Gene: ZNF772 HGNC NCBI

Linked Data

ClinVar Variation Id: 161496
ClinVar RCV Id: RCV000149030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019767.1:p.Ala4delinsGlyPro
CA174141
NM_001024596.3:c.10_11insGGC