Canonical Allele Identifier: PA2580524613
Gene: ZNF579 HGNC NCBI

Linked Data

ClinVar Variation Id: 2263119
ClinVar RCV Id: RCV004122121
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689813.2:p.Gln367His
CA9677400
NM_152600.3:c.1101G>T
CA407524436
NM_152600.3:c.1101G>C