Canonical Allele Identifier: PA2828272017
Gene: TBC1D32 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354688.1:p.Arg1145Thr
CA3980476
NM_001367759.1:c.3434G>C