Canonical Allele Identifier: PA156150
Gene: ZNF526 HGNC NCBI

Linked Data

ClinVar Variation Id: 130838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597701.1:p.Pro189Leu
CA156149
NM_133444.1:c.566C>T