Canonical Allele Identifier: PA916037642
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120287
ClinVar RCV Id: RCV000106368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.His271Leu
CA267675
NM_001354304.2:c.812A>T