Canonical Allele Identifier: PA2825137935
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 872833
ClinVar RCV Id: RCV001093505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu127Gly
CA16020782
NM_000277.3:c.380A>G