Canonical Allele Identifier: PA2825138031
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2388853
ClinVar RCV Id: RCV002714262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn223Ser
CA6748884
NM_000277.3:c.668A>G