Canonical Allele Identifier: PA916037437
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102657
ClinVar RCV Id: RCV000088904 RCV001384288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro122Gln
CA229524
NM_001354304.2:c.365C>A