Canonical Allele Identifier: PA916037670
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ile283Asn
CA229821
NM_001354304.2:c.848T>A