Canonical Allele Identifier: PA105193
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102885
ClinVar RCV Id: RCV000089146 RCV000993622
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg297Cys
CA229836
NM_000277.3:c.889C>T