Canonical Allele Identifier: PA106597
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102796
ClinVar RCV Id: RCV000089047 RCV000672442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr238Pro
CA229705
NM_000277.3:c.712A>C