Canonical Allele Identifier: PA2825137885
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2108149
ClinVar RCV Id: RCV003034020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser67Tyr
CA386304220
NM_000277.3:c.200C>A