Canonical Allele Identifier: PA105040
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 590772
ClinVar RCV Id: RCV000721919
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg157Asn
CA16020798
NM_000277.3:c.470_471delinsAC