Allele Registry

Canonical Allele Identifier: PA916037612

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000000633

RCV000089089

ClinVar Variation:

602

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ala259Val	CA229756 NM_001354304.2:c.776C>T