Allele Registry

Canonical Allele Identifier: PA2573271213

Gene: PHIP HGNC NCBI

ClinVar RCV:

RCV002249126

ClinVar Variation:

1685399

HGVS (amino-acid)	Matching Registered Transcripts
NP_060404.4:p.Phe17Cys	CA364652623 NM_017934.7:c.50T>G