Canonical Allele Identifier: PA229407
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102572
ClinVar RCV Id: RCV000088808 RCV001269318
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe410Cys
CA229406
NM_000277.3:c.1229T>G