Canonical Allele Identifier: PA658825349
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 552907
ClinVar RCV Id: RCV000668256 RCV000985880
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile406Met
CA6748708
NM_000277.3:c.1218A>G