Canonical Allele Identifier: PA916037370
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102601
ClinVar RCV Id: RCV000088842 RCV000490373 RCV001175359 RCV003398704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg53His
CA229447
NM_001354304.2:c.158G>A