Canonical Allele Identifier: PA916037433
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 92741
ClinVar RCV Id: RCV000178066 RCV000790751 RCV004019527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro119Ser
CA220582
NM_001354304.2:c.355C>T