Canonical Allele Identifier: PA1139727986
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 932260
ClinVar RCV Id: RCV001199986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala373Asp
CA16020943
NM_001354304.2:c.1118C>A