Canonical Allele Identifier: PA2741867153
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2677442
ClinVar RCV Id: RCV003476589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser310Cys
CA386291704
NM_001354304.2:c.929C>G