Allele Registry

Canonical Allele Identifier: PA229838

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089147

RCV000993623

ClinVar Variation:

102886

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Phe299del	CA229837 NM_000277.3:c.895_897del