Canonical Allele Identifier: PA229898
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102927
ClinVar RCV Id: RCV000089194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly332Glu
CA229897
NM_000277.3:c.995G>A