Canonical Allele Identifier: PA2826149519
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3212198
ClinVar RCV Id: RCV004501134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171825.1:p.Gly785Arg
CA413252742
NM_001184896.1:c.2353G>A
CA413252745
NM_001184896.1:c.2353G>C