Canonical Allele Identifier: PA2825138190
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 993142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro366Leu
CA386493309
NM_000277.3:c.1097C>T