Canonical Allele Identifier: PA229752
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102829
ClinVar RCV Id: RCV000089086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly257Asp
CA229751
NM_000277.3:c.770G>A