Canonical Allele Identifier: PA105842
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102699
ClinVar RCV Id: RCV000088947 RCV002514543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile164Thr
CA229578
NM_000277.3:c.491T>C