Canonical Allele Identifier: PA916037397
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120271
ClinVar RCV Id: RCV000106352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro69_Ser70dup
CA267647
NM_001354304.2:c.206_211dup