Canonical Allele Identifier: PA916037386
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102619
ClinVar RCV Id: RCV000088861 RCV000758120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Thr63Pro
CA229473
NM_001354304.2:c.187A>C