Canonical Allele Identifier: PA2825137882
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1056831
ClinVar RCV Id: RCV001365715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ser67Cys
CA386304219
NM_000277.3:c.200C>G