Canonical Allele Identifier: PA916037736
Gene: PAH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Phe331Ser
CA16020915
NM_001354304.2:c.992T>C