Canonical Allele Identifier: PA106137
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 872838
ClinVar RCV Id: RCV001093519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu62Pro
CA16020739
NM_000277.3:c.185T>C