Canonical Allele Identifier: PA106044
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu255Ser
CA229747
NM_000277.3:c.764T>C