Canonical Allele Identifier: PA2573071359
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327556
ClinVar RCV Id: RCV001789818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Thr328Asn
CA16020914
NM_001354304.2:c.983C>A