Canonical Allele Identifier: PA2580161081
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804980
ClinVar RCV Id: RCV002471398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171825.1:p.Arg809Pro
CA413252242
NM_001184896.1:c.2426G>C