Canonical Allele Identifier: PA2827462368
Gene: TMCO4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336042.1:p.Met67Ile
CA338809699
NM_001349113.3:c.201G>C
CA338809709
NM_001349113.3:c.201G>A
CA338809711
NM_001349113.3:c.201G>T