Allele Registry

Canonical Allele Identifier: PA658663651

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000553622

ClinVar Variation:

458078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Gly346Glu	CA16020921 NM_000277.3:c.1037G>A