Allele Registry

Canonical Allele Identifier: PA916071893

Gene: TAS2R38 HGNC NCBI

ClinVar Allele:

17943

ClinVar RCV:

RCV000003038

ClinVar Variation:

2904

HGVS (amino-acid)	Matching Registered Transcripts
NP_789787.5:p.Ala49Pro	CA115855 NM_176817.5:c.145G>C