Canonical Allele Identifier: PA229469
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102616
ClinVar RCV Id: RCV000088858 RCV000758114
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp59Gly
CA229468
NM_000277.3:c.176A>G