Canonical Allele Identifier: PA916037801
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 551270
ClinVar RCV Id: RCV000666283 RCV001779045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro384Ser
CA16020950
NM_001354304.2:c.1150C>T