Canonical Allele Identifier: PA916037563
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102786
ClinVar RCV Id: RCV000089037 RCV000190611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser231Pro
CA229694
NM_001354304.2:c.691T>C