Canonical Allele Identifier: PA2825138213
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2682167
ClinVar RCV Id: RCV003479540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu385Pro
CA16020951
NM_000277.3:c.1154T>C