Canonical Allele Identifier: PA2826704722
Gene: TBCE HGNC NCBI

Linked Data

ClinVar Variation Id: 3174779
ClinVar RCV Id: RCV004474127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274730.1:p.Glu427Asp
CA1464357
NM_001287801.2:c.1281G>C
CA344944629
NM_001287801.2:c.1281G>T