Canonical Allele Identifier: PA2825137995
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1513560
ClinVar RCV Id: RCV002018434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly188Ser
CA386296839
NM_000277.3:c.562G>A