Canonical Allele Identifier: PA105089
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 631
ClinVar RCV Id: RCV000000663 RCV000088974 RCV000346024 RCV001280536 RCV002251846 RCV002512614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg176Leu
CA114371
NM_000277.3:c.527G>T