Canonical Allele Identifier: PA105802
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102752
ClinVar RCV Id: RCV000089001 RCV000509208 RCV000588479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His201Tyr
CA229643
NM_000277.3:c.601C>T