Canonical Allele Identifier: PA913195012
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619157
ClinVar RCV Id: RCV000758113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp75Val
CA16020751
NM_000277.3:c.224A>T