Canonical Allele Identifier: PA913195171
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619161
ClinVar RCV Id: RCV000758124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu367Arg
CA16020939
NM_000277.3:c.1100T>G