Canonical Allele Identifier: PA916037436
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619155
ClinVar RCV Id: RCV000758109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Phe121Ser
CA16020779
NM_001354304.2:c.362T>C