Canonical Allele Identifier: PA106581
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 583
ClinVar RCV Id: RCV000000613 RCV000088884 RCV000763293 RCV002512609 RCV003934787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser87Arg
CA114359
NM_000277.3:c.261C>A
CA16020758
NM_000277.3:c.259A>C
CA386304103
NM_000277.3:c.261C>G