Canonical Allele Identifier: PA2741845434
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2558103
ClinVar RCV Id: RCV003295720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171825.1:p.Ser771Leu
CA329924353
NM_001184896.1:c.2312C>T