Canonical Allele Identifier: PA229843
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser303Ala
CA229842
NM_000277.3:c.907T>G