Canonical Allele Identifier: PA2573206011
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1402572
ClinVar RCV Id: RCV001896984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Glu21Asp
CA6749050
NM_001354304.2:c.63A>C
CA386302823
NM_001354304.2:c.63A>T