Canonical Allele Identifier: PA229693
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102785
ClinVar RCV Id: RCV000089036 RCV001789761
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Val230Gly
CA229692
NM_000277.3:c.689T>G