Canonical Allele Identifier: PA105812
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102834
ClinVar RCV Id: RCV000089093 RCV000758099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.His264Leu
CA229761
NM_000277.3:c.791A>T