Canonical Allele Identifier: PA2573071363
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327551
ClinVar RCV Id: RCV001789813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Tyr417Cys
CA16020983
NM_001354304.2:c.1250A>G