Canonical Allele Identifier: PA105907
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102876
ClinVar RCV Id: RCV000089137 RCV000169005
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile283Phe
CA229820
NM_000277.3:c.847A>T