Canonical Allele Identifier: PA658663496
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 451812
ClinVar RCV Id: RCV000522171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr189Arg
CA386296823
NM_000277.3:c.566C>G