Canonical Allele Identifier: PA229421
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102582
ClinVar RCV Id: RCV000088820 RCV001388783
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile421Thr
CA229420
NM_000277.3:c.1262T>C