Canonical Allele Identifier: PA267672
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120285
ClinVar RCV Id: RCV000106366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val262Gly
CA267671
NM_000277.3:c.785T>G