Canonical Allele Identifier: PA916037487
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102711
ClinVar RCV Id: RCV000088959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.His170Arg
CA229593
NM_001354304.2:c.509A>G