Canonical Allele Identifier: PA645420275
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 281073
ClinVar RCV Id: RCV000350174 RCV000721175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr328Ile
CA10603804
NM_000277.3:c.983C>T