Canonical Allele Identifier: PA916037607
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_001341233.1:p.Gly257Asp
CA229751
NM_001354304.2:c.770G>A