Allele Registry

Canonical Allele Identifier: PA891863295

Gene: PHIP HGNC NCBI

ClinVar RCV:

RCV000228040

RCV000656343

ClinVar Variation:

242321

HGVS (amino-acid)	Matching Registered Transcripts
NP_060404.4:p.Phe17Ser	CA10583977 NM_017934.7:c.50T>C