Allele Registry

Canonical Allele Identifier: PA916037783

Gene: PAH HGNC NCBI

ClinVar Allele:

108251

ClinVar RCV:

RCV000088748

RCV002514542

ClinVar Variation:

102515

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Pro362Thr	CA229332 NM_001354304.2:c.1084C>A