Allele Registry

Canonical Allele Identifier: PA1139732361

Gene: PHIP HGNC NCBI

ClinVar RCV:

RCV001253094

RCV001266056

RCV001526636

RCV002286830

RCV004538536

ClinVar Variation:

975951

HGVS (amino-acid)	Matching Registered Transcripts
NP_060404.4:p.Arg110Cys	CA142188117 NM_017934.7:c.328C>T