Canonical Allele Identifier: PA267674
Gene: PAH HGNC NCBI
ClinVar RCV:
RCV000106367
ClinVar Variation:
120286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr266Pro
CA267673
NM_000277.3:c.796A>C