Canonical Allele Identifier: PA229607
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102724
ClinVar RCV Id: RCV000088972 RCV000810165
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg176Gln
CA229606
NM_000277.3:c.527G>A