Canonical Allele Identifier: PA105989
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102742
ClinVar RCV Id: RCV000088991 RCV000411842
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu194Pro
CA229633
NM_000277.3:c.581T>C