Canonical Allele Identifier: PA229506
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile94Ser
CA229505
NM_000277.3:c.281T>G