Canonical Allele Identifier: PA2826149619
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1804980
ClinVar RCV Id: RCV002471398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171826.1:p.Arg672Pro
CA413252242
NM_001184897.2:c.2015G>C