Allele Registry

Canonical Allele Identifier: PA2825138181

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000988898

ClinVar Variation:

802886

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro362Arg	CA386493332 NM_000277.3:c.1085C>G