Canonical Allele Identifier: PA208732
Gene: ZNF711 HGNC NCBI

Linked Data

ClinVar Variation Id: 212693
ClinVar RCV Id: RCV000194519 RCV001166221 RCV002252048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068838.3:p.Ala277Thr
CA208731
NM_021998.5:c.829G>A