Canonical Allele Identifier: PA106812
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102784
ClinVar RCV Id: RCV000089035 RCV000411829 RCV003398705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val230Ile
CA286506
NM_000277.3:c.688G>A