Canonical Allele Identifier: PA916037840
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 617
ClinVar RCV Id: RCV000000648 RCV000088815 RCV000401074 RCV003415609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asp415Asn
CA114364
NM_001354304.2:c.1243G>A