Canonical Allele Identifier: PA106325
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102781
ClinVar RCV Id: RCV000089032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro225Arg
CA229688
NM_000277.3:c.674C>G