Allele Registry

Canonical Allele Identifier: PA916037391

Gene: PAH HGNC NCBI

ClinVar Allele:

15675

ClinVar RCV:

RCV000000668

RCV000078516

RCV002251847

RCV003398402

RCV004018528

ClinVar Variation:

636

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ile65Thr	CA251544 NM_001354304.2:c.194T>C