Canonical Allele Identifier: PA2825137862
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 972021
ClinVar RCV Id: RCV001247948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val45Phe
CA386302394
NM_000277.3:c.133G>T