Canonical Allele Identifier: PA2825137892
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1344578
ClinVar RCV Id: RCV002254727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Leu72_Asp75delinsTyr
CA2573147904
NM_000277.3:c.215_223del