Canonical Allele Identifier: PA916037841
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 558091
ClinVar RCV Id: RCV000674315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro416Gln
CA16020981
NM_001354304.2:c.1247C>A