Canonical Allele Identifier: PA2825137899
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 872831
ClinVar RCV Id: RCV001093503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu78Val
CA16020755
NM_000277.3:c.233A>T