Canonical Allele Identifier: PA2580404162
Gene: TMEM165 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060945.2:p.Pro28Ala
CA356958746
NM_018475.5:c.82C>G