Allele Registry

Canonical Allele Identifier: PA106643

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088818

RCV000672448

ClinVar Variation:

102580

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr418Pro	CA229418 NM_000277.3:c.1252A>C