Canonical Allele Identifier: PA916037404
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619158
ClinVar RCV Id: RCV000758118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asp75Gly
CA16020750
NM_001354304.2:c.224A>G