Canonical Allele Identifier: PA916037395
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102627
ClinVar RCV Id: RCV000088870 RCV001543636
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Arg68Gly
CA229484
NM_001354304.2:c.202A>G