Canonical Allele Identifier: PA2825137944
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2173312
ClinVar RCV Id: RCV002574572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala140Val
CA6748960
NM_000277.3:c.419C>T