Canonical Allele Identifier: PA1139728147
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 940659
ClinVar RCV Id: RCV001210291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg413His
CA6748707
NM_001354304.2:c.1238G>A