Canonical Allele Identifier: PA229708
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102798
ClinVar RCV Id: RCV000089049 RCV001857432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly239Asp
CA229707
NM_000277.3:c.716G>A