Canonical Allele Identifier: PA105135
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102823
ClinVar RCV Id: RCV000089078 RCV000674327
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Arg252Gly
CA229742
NM_000277.3:c.754C>G