Canonical Allele Identifier: PA915981452
Gene: ZNF772 HGNC NCBI

Linked Data

ClinVar Variation Id: 161496
ClinVar RCV Id: RCV000149030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137540.1:p.Ala4delinsGlyPro
CA174141
NM_001144068.1:c.10_11insGGC