Canonical Allele Identifier: PA106652
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102643
ClinVar RCV Id: RCV000088888 RCV001854512
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr92Ile
CA229504
NM_000277.3:c.275C>T