Canonical Allele Identifier: PA916037403
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 650381
ClinVar RCV Id: RCV000805522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asp75Asn
CA6748995
NM_001354304.2:c.223G>A