Canonical Allele Identifier: PA916037686
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102885
ClinVar RCV Id: RCV000089146 RCV000993622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg297Cys
CA229836
NM_001354304.2:c.889C>T