Canonical Allele Identifier: PA916037711
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 446506
ClinVar RCV Id: RCV000515773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gly312Cys
CA386291684
NM_001354304.2:c.934G>T