Allele Registry

Canonical Allele Identifier: PA312805

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV002000227

ClinVar Variation:

1453298

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Glu205Asp	CA312804 NM_000277.3:c.615G>C CA386296707 NM_000277.3:c.615G>T