Canonical Allele Identifier: PA104921
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 616
ClinVar RCV Id: RCV000000647 RCV000089177 RCV000675108 RCV002251845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala322Gly
CA114363
NM_000277.3:c.965C>G