Canonical Allele Identifier: PA2825138112
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805825
ClinVar RCV Id: RCV000993642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gln301Pro
CA16020889
NM_000277.3:c.902A>C