Canonical Allele Identifier: PA105918
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 618
ClinVar RCV Id: RCV000000649 RCV000089157 RCV000169485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile306Val
CA114365
NM_000277.3:c.916A>G