Allele Registry

Canonical Allele Identifier: PA891863299

Gene: PHIP HGNC NCBI

ClinVar RCV:

RCV000414004

ClinVar Variation:

373303

HGVS (amino-acid)	Matching Registered Transcripts
NP_060404.4:p.His182Arg	CA16042559 NM_017934.7:c.545A>G