Canonical Allele Identifier: PA916037790
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 625289
ClinVar RCV Id: RCV000850224

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu368Lys
CA386493305
NM_001354304.2:c.1102G>A