Canonical Allele Identifier: PA916037829
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 635
ClinVar RCV Id: RCV000000667 RCV000088804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Pro407Leu
CA229402
NM_001354304.2:c.1220C>T