Canonical Allele Identifier: PA916037465
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102691
ClinVar RCV Id: RCV000088939 RCV002513933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg157Ile
CA229567
NM_001354304.2:c.470G>T