Canonical Allele Identifier: PA1139727979
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 993142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro366Leu
CA386493309
NM_001354304.2:c.1097C>T