Canonical Allele Identifier: PA2825138011
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1491340
ClinVar RCV Id: RCV001986456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu205Gly
CA386296709
NM_000277.3:c.614A>G