Canonical Allele Identifier: PA2573071364
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327552
ClinVar RCV Id: RCV001789814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Tyr417Asp
CA16020982
NM_001354304.2:c.1249T>G