Canonical Allele Identifier: PA913195066
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619159
ClinVar RCV Id: RCV000758119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu258Pro
CA16020855
NM_000277.3:c.773T>C