Canonical Allele Identifier: PA267650
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 120272
ClinVar RCV Id: RCV000106353 RCV003390792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Ile95Thr
CA267649
NM_000277.3:c.284_285delinsCA
CA386304061
NM_000277.3:c.284T>C