Canonical Allele Identifier: PA229864
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102904
ClinVar RCV Id: RCV000089168 RCV000672630
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Pro314Thr
CA229863
NM_000277.3:c.940C>A