Canonical Allele Identifier: PA916037773
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102496
ClinVar RCV Id: RCV000088727 RCV001543661
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gly352Arg
CA229307
NM_001354304.2:c.1054G>C