Canonical Allele Identifier: PA916037610
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619159
ClinVar RCV Id: RCV000758119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Leu258Pro
CA16020855
NM_001354304.2:c.773T>C