Allele Registry

Canonical Allele Identifier: PA913195083

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000758104

ClinVar Variation:

619152

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.His271Gln	CA16020865 NM_000277.3:c.813T>G CA386294567 NM_000277.3:c.813T>A