Canonical Allele Identifier: PA2741867127
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2581597
ClinVar RCV Id: RCV003332002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu227Met
CA386296583
NM_001354304.2:c.679C>A