Allele Registry

Canonical Allele Identifier: PA106703

Gene: PAH HGNC NCBI

ClinVar Allele:

108596

ClinVar RCV:

RCV000089121

RCV000411640

ClinVar Variation:

102860

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Tyr277Cys	CA229800 NM_000277.3:c.830A>G