Canonical Allele Identifier: PA916037389
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102623
ClinVar RCV Id: RCV000088865 RCV000758100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ile65Asn
CA229479
NM_001354304.2:c.194T>A