Canonical Allele Identifier: PA229618
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102731
ClinVar RCV Id: RCV000088980 RCV001248714
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Glu182Gly
CA229617
NM_000277.3:c.545A>G