Canonical Allele Identifier: PA229646
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102754
ClinVar RCV Id: RCV000089003 RCV001543657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Cys203Tyr
CA229645
NM_000277.3:c.608G>A