Canonical Allele Identifier: PA2825370318
Gene: CSTF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3078437
ClinVar RCV Id: RCV004372750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028693.1:p.Lys287Arg
CA409398526
NM_001033521.2:c.860A>G