Canonical Allele Identifier: PA2825138093
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1458269
ClinVar RCV Id: RCV001972840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro281Arg
CA16020868
NM_000277.3:c.842C>G