Canonical Allele Identifier: PA916037426
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 551968
ClinVar RCV Id: RCV000667147

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gly103Ser
CA16020763
NM_001354304.2:c.307G>A