Canonical Allele Identifier: PA916037853
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102585
ClinVar RCV Id: RCV000088824 RCV001789756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu430Pro
CA229426
NM_001354304.2:c.1289T>C