Canonical Allele Identifier: PA916037477
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92743
ClinVar RCV Id: RCV000078523 RCV000412232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asn167Ile
CA220584
NM_001354304.2:c.500A>T