Canonical Allele Identifier: PA229804
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102863
ClinVar RCV Id: RCV000089124 RCV000672785
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr278Ile
CA229803
NM_000277.3:c.833C>T