Canonical Allele Identifier: PA916037466
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102693
ClinVar RCV Id: RCV000409986 RCV000088941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg158Trp
CA229570
NM_001354304.2:c.472C>T