Canonical Allele Identifier: PA2829778793
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804980
ClinVar RCV Id: RCV002471398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055922.1:p.Arg773Pro
CA413252242
NM_015107.3:c.2318G>C