Canonical Allele Identifier: PA916037447
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102668
ClinVar RCV Id: RCV000088916
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.His146Tyr
CA229540
NM_001354304.2:c.436C>T