Canonical Allele Identifier: PA2580533018
Gene: TAS2R38 HGNC NCBI

Linked Data

ClinVar Variation Id: 2495751
ClinVar RCV Id: RCV004283279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789787.5:p.Val156Ala
CA369564859
NM_176817.5:c.467T>C