Canonical Allele Identifier: PA105822
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102849
ClinVar RCV Id: RCV000089108 RCV000758116 RCV002287367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His271Tyr
CA229784
NM_000277.3:c.811C>T