Allele Registry

Canonical Allele Identifier: PA104874

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000000633

RCV000089089

ClinVar Variation:

602

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ala259Val	CA229756 NM_000277.3:c.776C>T