Canonical Allele Identifier: PA916037550
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 549912
ClinVar RCV Id: RCV000664486 RCV003420168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asn223Ile
CA6748885
NM_001354304.2:c.668A>T