Canonical Allele Identifier: PA354152
Gene: PAH HGNC NCBI
ClinVar RCV:
RCV000210807
ClinVar Variation:
225134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His107Arg
CA354151
NM_000277.3:c.320A>G