Canonical Allele Identifier: PA106263
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe39Leu
CA251537
NM_000277.3:c.117C>G
CA386302494
NM_000277.3:c.117C>A
CA386302507
NM_000277.3:c.115T>C