Canonical Allele Identifier: PA916037575
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102801
ClinVar RCV Id: RCV000089052 RCV000667600 RCV002514546 RCV004525872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Phe240Val
CA229713
NM_001354304.2:c.718T>G