Canonical Allele Identifier: PA1139741986
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 872832
ClinVar RCV Id: RCV001093504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Phe121Val
CA16020778
NM_001354304.2:c.361T>G