Canonical Allele Identifier: PA105884
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102842
ClinVar RCV Id: RCV000089101 RCV000281383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile269Leu
CA229775
NM_000277.3:c.805A>C