Canonical Allele Identifier: PA916037560
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Val230Gly
CA229692
NM_001354304.2:c.689T>G