Canonical Allele Identifier: PA2825137836
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2167364
ClinVar RCV Id: RCV003099019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asn8Asp
CA6749065
NM_000277.3:c.22A>G