Canonical Allele Identifier: PA2825138126
Gene: PAH HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly312Val
CA16020902
NM_000277.3:c.935G>T