Canonical Allele Identifier: PA105426
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102639
ClinVar RCV Id: RCV000088883 RCV000761308
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp84Tyr
CA229500
NM_000277.3:c.250G>T