Canonical Allele Identifier: PA916037819
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120263
ClinVar RCV Id: RCV000106344 RCV002287368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Val399Ala
CA267634
NM_001354304.2:c.1196T>C