Canonical Allele Identifier: PA1139741973
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 883981
ClinVar RCV Id: RCV001114785 RCV003226435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ile94Val
CA6748988
NM_001354304.2:c.280A>G