Canonical Allele Identifier: PA105080
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102706
ClinVar RCV Id: RCV000088954 RCV000311018 RCV001530926 RCV002515783 RCV003987362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg169His
CA286505
NM_000277.3:c.506G>A