Canonical Allele Identifier: PA106605
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102861
ClinVar RCV Id: RCV000089122 RCV001789762
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr278Ala
CA229801
NM_000277.3:c.832A>G