Allele Registry

Canonical Allele Identifier: PA2825138052

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV002005780

ClinVar Variation:

1484418

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg241Ser	CA386295836 NM_000277.3:c.721C>A