Canonical Allele Identifier: PA1139741904
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 880692
ClinVar RCV Id: RCV001109151

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu15His
CA386303822
NM_001354304.2:c.44T>A