Canonical Allele Identifier: PA916037693
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Ala300Val
CA229839
NM_001354304.2:c.899C>T