Canonical Allele Identifier: PA2826149682
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10798
ClinVar RCV Id: RCV000011545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171827.1:p.Arg211Ter