Canonical Allele Identifier: PA106712
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92756
ClinVar RCV Id: RCV000078541 RCV000150081
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr325Cys
CA220593
NM_000277.3:c.974A>G