Allele Registry

Canonical Allele Identifier: PA105884

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089101

RCV000281383

ClinVar Variation:

102842

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile269Leu	CA229775 NM_000277.3:c.805A>C