Canonical Allele Identifier: PA2825138141
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2682170
ClinVar RCV Id: RCV003479543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile324Asn
CA10602335
NM_000277.3:c.971T>A