Canonical Allele Identifier: PA2825138196
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1327564
ClinVar RCV Id: RCV001789826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu369Val
CA16020941
NM_000277.3:c.1105C>G