Canonical Allele Identifier: PA916037812
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102544
ClinVar RCV Id: RCV000088778 RCV001269040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Phe392Ser
CA229369
NM_001354304.2:c.1175T>C