Canonical Allele Identifier: PA220581
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ala104_Val106del
CA220580
NM_000277.3:c.310_318del