Allele Registry

Canonical Allele Identifier: PA2741867145

Gene: PAH HGNC NCBI

ClinVar Allele:

3051928

ClinVar RCV:

RCV003597939

ClinVar Variation:

2891786

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Pro279Thr	CA386294537 NM_001354304.2:c.835C>A