Canonical Allele Identifier: PA916037604
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 600
ClinVar RCV Id: RCV000000631 RCV000089083
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu255Ser
CA229747
NM_001354304.2:c.764T>C