Allele Registry

Canonical Allele Identifier: PA106571

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088867

RCV001260324

ClinVar Variation:

102625

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser67Pro	CA229481 NM_000277.3:c.199T>C