Allele Registry

Canonical Allele Identifier: PA106652

Gene: PAH HGNC NCBI

ClinVar Allele:

108379

ClinVar RCV:

RCV000088888

RCV001854512

ClinVar Variation:

102643

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr92Ile	CA229504 NM_000277.3:c.275C>T