Canonical Allele Identifier: PA106552
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102494
ClinVar RCV Id: RCV000088725 RCV001543633
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser350Thr
CA229304
NM_000277.3:c.1048T>A