Canonical Allele Identifier: PA229714
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102801
ClinVar RCV Id: RCV000089052 RCV000667600 RCV002514546 RCV004525872
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Phe240Val
CA229713
NM_000277.3:c.718T>G