Canonical Allele Identifier: PA2741867107
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2677436
ClinVar RCV Id: RCV003471653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg169Leu
CA386299454
NM_001354304.2:c.506G>T