Canonical Allele Identifier: PA916037782
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 802886
ClinVar RCV Id: RCV000988898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro362Arg
CA386493332
NM_001354304.2:c.1085C>G