Canonical Allele Identifier: PA106225
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102802
ClinVar RCV Id: RCV000089053 RCV002259590
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe240Ser
CA229715
NM_000277.3:c.719T>C