Canonical Allele Identifier: PA2826149741
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504702
ClinVar RCV Id: RCV003234293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171827.1:p.Gln702Pro
CA413253333
NM_001184898.2:c.2105A>C