Canonical Allele Identifier: PA105161
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102832
ClinVar RCV Id: RCV000089091 RCV000410877
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg261Pro
CA229759
NM_000277.3:c.782G>C