Canonical Allele Identifier: PA105685
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102818
ClinVar RCV Id: RCV000089073 RCV000169396
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly247Val
CA229736
NM_000277.3:c.740G>T