Canonical Allele Identifier: PA2825138205
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1714193
ClinVar RCV Id: RCV002297173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn376Ser
CA386493256
NM_000277.3:c.1127A>G