Canonical Allele Identifier: PA645407583
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 286532
ClinVar RCV Id: RCV000261029
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171825.1:p.Asp21Gly
CA10605495
NM_001184896.1:c.62A>G