Canonical Allele Identifier: PA916037398
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102628
ClinVar RCV Id: RCV000088871 RCV003315609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro69Ser
CA229486
NM_001354304.2:c.205C>T