Canonical Allele Identifier: PA2826149757
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804980
ClinVar RCV Id: RCV002471398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171827.1:p.Arg756Pro
CA413252242
NM_001184898.2:c.2267G>C