Allele Registry

Canonical Allele Identifier: PA916037430

Gene: PAH HGNC NCBI

ClinVar Allele:

108387

ClinVar RCV:

RCV000088897

RCV002259587

ClinVar Variation:

102651

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ser110Leu	CA229516 NM_001354304.2:c.329C>T