Canonical Allele Identifier: PA916037349
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102757
ClinVar RCV Id: RCV000089006 RCV000993618
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gln20His
CA229651
NM_001354304.2:c.60G>C
CA386303792
NM_001354304.2:c.60G>T