Canonical Allele Identifier: PA2825138254
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327551
ClinVar RCV Id: RCV001789813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr417Cys
CA16020983
NM_000277.3:c.1250A>G