Canonical Allele Identifier: PA916037585
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102811
ClinVar RCV Id: RCV000089064 RCV000632879
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Val245Glu
CA229725
NM_001354304.2:c.734T>A