Canonical Allele Identifier: PA2580231141
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2152160
ClinVar RCV Id: RCV003061591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu214Gly
CA386296655
NM_001354304.2:c.641A>G