Canonical Allele Identifier: PA2825137877
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 971992
ClinVar RCV Id: RCV001559695 RCV001247911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Thr63_His64delinsProAsn
CA16020741
NM_000277.3:c.187_190delinsCCCA