Canonical Allele Identifier: PA2826149601
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504702
ClinVar RCV Id: RCV003234293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171826.1:p.Gln618Pro
CA413253333
NM_001184897.2:c.1853A>C