Allele Registry

Canonical Allele Identifier: PA105773

Gene: PAH HGNC NCBI

ClinVar Allele:

98651

ClinVar RCV:

RCV000078524

RCV000150088

ClinVar Variation:

92744

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.His170Asp	CA273111 NM_000277.3:c.508C>G