Canonical Allele Identifier: PA2499251822
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1185012
ClinVar RCV Id: RCV001543655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu368Gly
CA16020940
NM_001354304.2:c.1103A>G