Canonical Allele Identifier: PA2580231002
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2108149
ClinVar RCV Id: RCV003034020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ser67Tyr
CA386304220
NM_001354304.2:c.200C>A