Allele Registry

Canonical Allele Identifier: PA891863296

Gene: PHIP HGNC NCBI

ClinVar RCV:

RCV000656347

ClinVar Variation:

545397

HGVS (amino-acid)	Matching Registered Transcripts
NP_060404.4:p.Arg110Ser	CA364651200 NM_017934.7:c.328C>A