Canonical Allele Identifier: PA2573071350
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327564
ClinVar RCV Id: RCV001789826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu369Val
CA16020941
NM_001354304.2:c.1105C>G