Canonical Allele Identifier: PA113469
Gene: PHF6 HGNC NCBI
ClinVar Allele:
26108
ClinVar RCV:
RCV000011818
ClinVar Variation:
11069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015877.1:p.Arg257Gly
CA121340
NM_001015877.2:c.769A>G