Canonical Allele Identifier: PA2825138103
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805822
ClinVar RCV Id: RCV000993639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp296His
CA16020885
NM_000277.3:c.886G>C