Canonical Allele Identifier: PA2825138128
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1474010
ClinVar RCV Id: RCV001970975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp315Glu
CA386291635
NM_000277.3:c.945T>G
CA386291637
NM_000277.3:c.945T>A