Canonical Allele Identifier: PA658825291
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 549912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn223Ile
CA6748885
NM_000277.3:c.668A>T