Canonical Allele Identifier: PA2825138197
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 625290
ClinVar RCV Id: RCV000850225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu370Gly
CA386493290
NM_000277.3:c.1109A>G