Canonical Allele Identifier: PA2826149605
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2558103
ClinVar RCV Id: RCV003295720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171826.1:p.Ser634Leu
CA329924353
NM_001184897.2:c.1901C>T