Canonical Allele Identifier: PA2825138239
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 2428043
ClinVar RCV Id: RCV003117014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala404Ser
CA386493099
NM_000277.3:c.1210G>T