Canonical Allele Identifier: PA916037755
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102477
ClinVar RCV Id: RCV000088708 RCV001194126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Tyr343Cys
CA229282
NM_001354304.2:c.1028A>G