Canonical Allele Identifier: PA916037695
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 805825
ClinVar RCV Id: RCV000993642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Gln301Pro
CA16020889
NM_001354304.2:c.902A>C