Canonical Allele Identifier: PA2828271991
Gene: TBC1D32 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354688.1:p.Lys934Met
CA146024006
NM_001367759.1:c.2801A>T