Canonical Allele Identifier: PA2825138032
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2139677
ClinVar RCV Id: RCV003052722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile224Leu
CA386296594
NM_000277.3:c.670A>C