Allele Registry

Canonical Allele Identifier: PA891863303

Gene: PHIP HGNC NCBI

ClinVar RCV:

RCV000490131

RCV000770903

ClinVar Variation:

426892

HGVS (amino-acid)	Matching Registered Transcripts
NP_060404.4:p.Ser287Tyr	CA364638305 NM_017934.7:c.860C>A