Canonical Allele Identifier: PA106742
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102538
ClinVar RCV Id: RCV000088771 RCV000169306 RCV003162523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr386Cys
CA274152
NM_000277.3:c.1157A>G