Canonical Allele Identifier: PA113469
Gene: PHF6 HGNC NCBI

Linked Data

ClinVar Variation Id: 11069
ClinVar RCV Id: RCV000011818
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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