Canonical Allele Identifier: PA2825138017
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2152160
ClinVar RCV Id: RCV003061591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu214Gly
CA386296655
NM_000277.3:c.641A>G