Allele Registry

Canonical Allele Identifier: PA2573206026

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001990771

ClinVar Variation:

1478759

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Arg53Ser	CA6749039 NM_001354304.2:c.157C>A