Canonical Allele Identifier: PA2826149614
Gene: PHF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 986145
ClinVar RCV Id: RCV001267403
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171826.1:p.Asn666Asp
CA10423311
NM_001184897.2:c.1996A>G