Canonical Allele Identifier: PA916037684
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805822
ClinVar RCV Id: RCV000993639
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Asp296His
CA16020885
NM_001354304.2:c.886G>C