Canonical Allele Identifier: PA916037810
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 225136
ClinVar RCV Id: RCV000210788
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser391Thr
CA357240
NM_001354304.2:c.1172G>C