Canonical Allele Identifier: PA229572
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102694
ClinVar RCV Id: RCV000088942 RCV000758092
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg158Pro
CA229571
NM_000277.3:c.473G>C