Canonical Allele Identifier: PA916037400
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102631
ClinVar RCV Id: RCV000088874 RCV002259586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser70Pro
CA229488
NM_001354304.2:c.208T>C