Canonical Allele Identifier: PA2742019463
Gene: TAS2R38 HGNC NCBI

Linked Data

ClinVar Variation Id: 2517014
ClinVar RCV Id: RCV004289746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789787.5:p.Thr217Pro
CA4520178
NM_176817.5:c.649A>C