Canonical Allele Identifier: PA105382
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102468
ClinVar RCV Id: RCV000088699 RCV000794431
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Asp338Tyr
CA229269
NM_000277.3:c.1012G>T