Canonical Allele Identifier: PA2825138063
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2691864
ClinVar RCV Id: RCV003494061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala259Gly
CA386295500
NM_000277.3:c.776C>G