Canonical Allele Identifier: PA105513
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102891
ClinVar RCV Id: RCV000089153 RCV001543640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gln304Arg
CA229844
NM_000277.3:c.911A>G