Canonical Allele Identifier: PA916037405
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu76Ala
CA229492
NM_001354304.2:c.227A>C