Canonical Allele Identifier: PA913195011
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 619158
ClinVar RCV Id: RCV000758118
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp75Gly
CA16020750
NM_000277.3:c.224A>G