Canonical Allele Identifier: PA2825138217
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327553
ClinVar RCV Id: RCV001789815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr387Asp
CA16020952
NM_000277.3:c.1159T>G