Canonical Allele Identifier: PA229308
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102496
ClinVar RCV Id: RCV000088727 RCV001543661
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly352Arg
CA229307
NM_000277.3:c.1054G>C