Canonical Allele Identifier: PA2825138223
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2137404
ClinVar RCV Id: RCV003062533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser391Ile
CA16020957
NM_000277.3:c.1172G>T