Canonical Allele Identifier: PA105320
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp129Tyr
CA286503
NM_000277.3:c.385G>T