Canonical Allele Identifier: PA2825138182
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2735932
ClinVar RCV Id: RCV003494677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro362Leu
CA16020937
NM_000277.3:c.1085C>T