Canonical Allele Identifier: PA2825370328
Gene: CSTF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2237726
ClinVar RCV Id: RCV004098700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028694.1:p.Asp290Asn
CA409398546
NM_001033522.2:c.868G>A