Canonical Allele Identifier: PA916037503
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102728
ClinVar RCV Id: RCV000088977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu178Val
CA229611
NM_001354304.2:c.533A>T