Canonical Allele Identifier: PA2826149740
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2630649
ClinVar RCV Id: RCV003402456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171827.1:p.Ala697Ser
CA413253432
NM_001184898.2:c.2089G>T